| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs191358957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635851 | AAACCTAATTTAAAT[A/G]GTGAAGAGTTGCCAA | 4215 |
| rs191365548 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631659 | GTTTGTGTTCTGGGT[G/T]TTGGCCAGTTGTTTT | 4215 |
| rs191370298 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629903 | AGCTCTTATAATAGC[A/G]TCATCTTATACAGAA | 4215 |
| rs191372022 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670749 | TCCAGGCAGGGGATG[C/T]TACAAGAGCAGAGAC | 4215 |
| rs191372769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678116 | ACAAAGCCTGTTTTC[C/T]CGCTTCGGCCCCACC | 4215 |
| rs191379733 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672112 | ACATGGTGAAACCCC[A/C/G]TCTCTATGAAAAATA | 4215 |
| rs191397761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678489 | CCAGCAAAATTCTAT[G/T]CCTGTTTTCAGAGCA | 4215 |
| rs191581760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653687 | TGTTTGCCCTTTAAA[C/G]CCTGCACTGTCAAGA | 4215 |
| rs191709575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660391 | TTTTTTTTTTAATTG[C/T]TTGTAGAGACAGGGT | 4215 |
| rs191907508 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654625 | CTCTAACTTTTTGAG[G/T]AACTGCCCAGATTTT | 4215 |
| rs191931213 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687131 | AGCACTTTGGGAAGC[C/T]GAGGCACGCGGATCA | 4215 |
| rs191934192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665034 | GCAGCTGGGCATGGT[C/T]GCTCACCCCTGTAAT | 4215 |
| rs191945892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644334 | ATTCTCCTGCCTCAG[A/C]CTCCCGAGTAGCTGG | 4215 |
| rs191947835 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672909 | GAAACAGAGACAGAA[A/G]TCAAGGTATAGCATG | 4215 |
| rs191951676 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623591 | GAAGATGTAATCTAA[A/G]GAAAGCTTTTAATGT | 4215 |
| rs191953400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669107 | ATGTGGCAAGAGAAT[G/T]GGCTGAGCCTGTGAG | 4215 |
| rs191981181 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627247 | CTTGTTTGATAGATC[C/G]TTTTCTAGTTCCATG | 4215 |
| rs191992791 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662718 | GTTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 4215 |
| rs192002028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638628 | TCTCACCGGATTGCC[A/T]GTGGTGGGGAGGGGA | 4215 |
| rs192095725 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667551 | AGGAGACTATTGACA[C/T]AGTACAGTCATTTCT | 4215 |
| rs192213096 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665407 | CCTGACCTCATGATC[C/T]GCCCGCCTCAGCCTC | 4215 |
| rs192258956 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687564 | GCATGGTGGCACATG[C/G]CTGTAGTCCCAGCTA | 4215 |
| rs192279287 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687945 | TCTCAAAAAAAAAAA[A/G]AGTCTGGCCCTGTCT | 4215 |
| rs192386060 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661939 | AACCCCATCTCTACT[A/G]AAAAATACAAAAAAT | 4215 |
| rs192462187 | snp | A/G | 0.000461422 | 0.0151822 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691798 | GACCCGAAAGTACAC[A/G]CGGCAGATCCTGGAG | 4215 |
| rs192480663 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647893 | AATTAGAATTCACAG[A/G]AAAGAGGAAAGAAGT | 4215 |
| rs192523155 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624810 | AGGGGAAAGTAGATG[A/T]CCTTGATACACTGTT | 4215 |
| rs192634159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681964 | AGCTCATAACAAGGG[A/G]TTCTTAGTAGTCACA | 4215 |
| rs192700629 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665858 | CAGCTGAACTCTCCC[C/T]TGAGAGCAGGAAACC | 4215 |
| rs192744794 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679674 | GTAGAGATGGGGTCT[C/G]ACCATGTTGCCCATG | 4215 |
| rs192760757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674675 | CTTAGGCTAGAGATA[G/T]GAGGAAGTGTATGAA | 4215 |
| rs192790439 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633932 | ATAAGGCCCTAAAAC[G/T]TTTCCTGTCTGTGGT | 4215 |
| rs192809510 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649259 | CTGGCCAACATGGTG[A/G]AACCCTGTCTCTACT | 4215 |
| rs192816801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680311 | GGAATGGAGGGCTCT[A/T]GTGTCTCTGGTTTTC | 4215 |
| rs192876142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637783 | GGAATCCTTATTTCC[A/G]TGGATTCCTGTTTCC | 4215 |
| rs192942195 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624262 | TATTATAGATTTTGA[A/G]TAAATCTTCGAATTG | 4215 |
| rs192972221 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655800 | CTACTTGGTTTTTTT[A/T]ATTTAACTCCCTTCC | 4215 |
| rs193026664 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628630 | CTCCCAAAGTGCTGG[G/T]ATTACAGGCGTGAGC | 4215 |
| rs193131254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63670153 | TGTGCCAGAAATATG[A/G]GAAGCAAAAAAGACA | 4215 |
| rs193140850 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629224 | GCCTCCTGTGTTCAG[A/G]CAATTCTCCTGCCTC | 4215 |
| rs193170349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645111 | TCTTCAATTCATTCA[A/G]CCACTTAACAAATAT | 4215 |
| rs193282344 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693126 | AGGCAAGGAAACAGG[C/T]TCTCCCCTCAGAGCC | 4215 |
| rs193297955 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649539 | GTCCTCCTGCCTCAA[C/T]CTCCCAGGTGCCTGG | 4215 |
| rs199506647 | in-del | -/CA | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679218 | CTGTTCCTAAAAGTG[-/CA]CACACACACACAGAG | 4215 |
| rs199571831 | snp | A/G | 5.3873e-05 | 0.00518976 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689571 | TTCCCCGAATACGGC[A/G]TCATCAAGGCAACTT | 4215 |
| rs199649595 | in-del | -/AAAAC | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629580 | GAAGGAAAAAAAACA[-/AAAAC]AAAACCTCAATCCAG | 4215 |
| rs199668197 | snp | A/C/G | 0.000895568 | 0.0211422 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693827 | GCTGCATGGCAGGGG[A/C/G]CTGCTGCTGGGCTCA | 4215 |
| rs199702580 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642373 | CTAAATATAATGTTG[G/T]CCCAGGGCTGGGGCA | 4215 |
| rs199864426 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660209 | ATTCCTTTATTTCCC[-/T]TTTTTTTTTGAGATG | 4215 |
| rs199910953 | snp | C/T | 0.00036248 | 0.0134577 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632746 | ATGAACCGACGTCAC[C/T]GGATGCCTGGATATG | 4215 |
| rs199943109 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654941 | CTCAGGAGCCTGAGG[C/G]AGAAGAATTACTTGA | 4215 |
| rs200012943 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665022 | AAATCTCCACAGGCA[C/G]CTGGGCATGGTCGCT | 4215 |
| rs200019744 | snp | C/T | 1.68832e-05 | 0.00290539 | synonymous-codon, intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692387 | CCCTGAGGTGATCAG[C/T]GGCGAGGGCTATGGA | 4215 |
| rs200150124 | snp | C/T | 1.70502e-05 | 0.00291972 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652674 | GAGAAGGCAGATGGA[C/T]GGGGCAGGGACAAGA | 4215 |
| rs200161650 | snp | C/T | 6.63889e-05 | 0.00576108 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693761 | TCACACACCACTTTG[C/T]ACAGCTCATGTACTG | 4215 |
| rs200168836 | snp | A/G | 0.00199799 | 0.0315437 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634725 | AAAAACACAACAGCA[A/G]CAGCTCAGCCCTTCT | 4215 |
| rs200191703 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685567 | GTCTGGAAGCTGCCA[A/G]TCCTTGGACAGGTCA | 4215 |
| rs200260705 | snp | C/T | 0.000807229 | 0.0200739 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667032 | TATCTACCAGCCCCC[C/T]GAGCCCAGAAGCAGG | 4215 |
| rs200364244 | snp | A/G/T | 3.29554e-05 | 0.00405914 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688789 | CCCTGTCTTACTCAG[A/G/T]TCGGGAAACTCAGCT | 4215 |
| rs200388532 | in-del | -/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687209 | GTCTCTACTAAAAAT[-/G]GAAAAAAAAAAAAAA | 4215 |
| rs200464376 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650850 | GCATGTACTATCACA[C/T]CTGGCTAATTTTTTA | 4215 |
| rs200616621 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655451 | TTTCTTCTTTTAATA[A/G]CCATCCTAGTAGGTG | 4215 |
| rs200666716 | in-del | -/AAA | 0.0232847 | 0.105357 | cds-indel | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695940 | ATAACTAATCCAGAT[-/AAA]AAGTTGTGGGGCTTC | 4215 |
| rs200763634 | snp | C/G | 5.05335e-05 | 0.00502635 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634671 | TTATGTTGCACGAAG[C/G]ATACAAATTATTAAC | 4215 |
| rs200804576 | snp | A/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63695089 | GAGTTGTCATTAAAG[A/G]AAAAAAAAAAAAAAA | 4215 |
| rs200819897 | snp | A/T | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681133 | AAAAAAAAAAAAAGG[A/T]AATATCATTACTCAT | 4215 |
| rs200856290 | in-del | -/G | 0.404035 | 0.196909 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670605 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAGAAA | 4215 |
| rs200867133 | in-del | -/AAG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649447 | AAAAAAAAAAAAAAA[-/AAG]TAGACAGGATCTCTG | 4215 |
| rs200955844 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661571 | TATCAAGCTGAACCT[C/T]CTTTTGTAACTTGTA | 4215 |
| rs200968266 | snp | A/G | 0.000215963 | 0.0103892 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692337 | ATGTCGGGGACGGGC[A/G]TGCGCTCCGTCACTG | 4215 |
| rs201065085 | snp | C/T | 1.64928e-05 | 0.00287161 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632816 | AGGTGTGTGTGACCC[C/T]GGCAGAGCTAAGTGA | 4215 |
| rs201079370 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637212 | AAAAAAAAAAAAAAA[C/T]AGTACTGGCCTAGGA | 4215 |
| rs201086636 | snp | A/G | 0.00199804 | 0.0315441 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681755 | TTGAAAGCCTCCTTT[A/G]TGTGCTCTAGGCTCC | 4215 |
| rs201087141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636114 | TGTGGGTTCATTAAC[A/G]GGATTGTTTGGGTGC | 4215 |
| rs201293817 | in-del | -/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655011 | CATTTGAGACAGAGT[-/C]TGAGACTCTGTCTCA | 4215 |
| rs201343358 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663501 | GCGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 4215 |
| rs201376513 | snp | C/G | 0.00062727 | 0.0176986 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690389 | CAGGTCCAATTTGAT[C/G]CAGACAGTCCTGAGA | 4215 |
| rs201427854 | snp | C/T | 3.29968e-05 | 0.00406169 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688537 | TCCAGCCCATCCTTC[C/T]GGAAATCACGAATGT | 4215 |
| rs201458544 | snp | C/T | 0.000405069 | 0.0142257 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689685 | GGCGCCTGCGGAGTG[C/T]GGACAGCGAGAATGC | 4215 |
| rs201464511 | snp | A/G | 3.31334e-05 | 0.00407009 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693719 | TTTTTGTGGAGGCTC[A/G]CCAGAGACCTTCAGC | 4215 |
| rs201466405 | in-del | -/AG | 0.046775 | 0.145601 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627631 | ATTTTTAGTAGAGAC[-/AG]GGTTTCACCATGTTG | 4215 |
| rs201478965 | snp | A/G | 5.00121e-05 | 0.00500035 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691907 | CAGGACCTGGGTTCA[A/G]GTCTACCATTGAGTG | 4215 |
| rs201554461 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687198 | TAGCGAAACCCCGTC[G/T]CTACTAAAAATGAAA | 4215 |
| rs201575395 | in-del | -/AG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649448 | AAAAAAAAAAAAAAA[-/AG]TAGACAGGATCTCTG | 4215 |
| rs201610357 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689033 | AGACAGGAAAAAAAC[-/A]AAAACAAAAACAGGG | 4215 |
| rs201618030 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662854 | TGGAGATGGGGTTGG[-/A]GCGGGGGGCGGTCCT | 4215 |
| rs201666054 | in-del | -/TA | 0.0138799 | 0.0821421 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696151 | CACCCACCCCAGCTC[-/TA]TGTCTGTGTCTGAAT | 4215 |
| rs201709115 | snp | A/G | 0.00011532 | 0.00759255 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667013 | CCGCAGGGGATATAA[A/G]TACTATCTACCAGCC | 4215 |
| rs201713792 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690319 | GGGCCAGGGTGCCTT[C/T]GGCAGGGTCTATTTG | 4215 |
| rs201722871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681724 | CCTCTTGGGCCACAC[A/T]CCCTGGGCTCTGTTG | 4215 |
| rs201730841 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645778 | AGCTAGAAACAGCAT[A/G]TCACAGCATAGCAAC | 4215 |
| rs201760686 | snp | C/T | 8.24287e-05 | 0.00641931 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632712 | GAACTCAATCATGAA[C/T]GATCTGGTGGCCCTC | 4215 |
| rs201848267 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633230 | GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 4215 |
| rs201868074 | in-del | -/A | 0.0275645 | 0.114116 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657623 | ATTGTACATTTAGAG[-/A]AAAAAAATCTGTATG | 4215 |
| rs202050738 | snp | C/T | 6.58946e-05 | 0.0057396 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666999 | CAAGGCTTCCCAGTC[C/T]GCAGGGGATATAAAT | 4215 |
| rs202109501 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654940 | ACTCAGGAGCCTGAG[A/G]CAGAAGAATTACTTG | 4215 |
| rs202150596 | snp | C/G | 0.00097802 | 0.0220928 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681910 | AGTGCGTGAGTATAG[C/G]GGGGCTGGGATATGC | 4215 |
| rs202160737 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692388 | CCTGAGGTGATCAGC[A/G]GCGAGGGCTATGGAA | 4215 |
| rs202202112 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670609 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 4215 |
| rs202203066 | snp | A/G | 1.73622e-05 | 0.00294632 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652684 | ATGGATGGGGCAGGG[A/G]CAAGAGGGGCAGATG | 4215 |
| rs367582628 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628391 | TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 4215 |
| rs367593101 | snp | C/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682863 | CAGGTTCTACTTGCA[C/G]TAAAGGGAAAGGCAG | 4215 |
| rs367679078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678478 | AGACAGGAAATCCAG[C/T]AAAATTCTATGCCTG | 4215 |
| rs367690477 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692075 | ATGGTCATTTTGTGC[A/G]GTAGATCTGAGACTC | 4215 |
| rs367720019 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691832 | ATGTCCTACCTGCAC[A/G]GCAACATGATTGTTC | 4215 |
| rs367727461 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646449 | CTCCTGTGATATGGT[G/T]CCATTACTATTCCCA | 4215 |
| rs367828176 | snp | G/T | 0.369958 | 0.21934 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650696 | AGAGAGAGAGAGAGA[G/T]TTTTTTTTTTTTTTA | 4215 |
| rs367877534 | snp | A/G | 2.56868e-05 | 0.00358368 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689499 | ACGTTCCGCCTCGTA[A/G]CCTGGGGTGTGACTT | 4215 |
| rs367877751 | snp | A/C | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687350 | CTCTACTAAAAAATA[A/C]AAAAAAAAAAAAAAT | 4215 |
| rs367893213 | snp | C/T | 6.71829e-05 | 0.00579542 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690441 | GTGGTCTGACTTCAG[C/T]TCCCTCCTTTCAACA | 4215 |
| rs367893756 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652845 | GGAGATTACTCAGCC[A/G]TCTCAGCCATCTCCA | 4215 |
| rs367901029 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632667 | CTTAGTCCATGTGCT[C/T]TCTTTCATTGCAGAC | 4215 |
| rs367914417 | snp | C/T | 3.30077e-05 | 0.00406236 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667050 | GCCCAGAAGCAGGCA[C/T]CTCTCTGTCAGTGAG | 4215 |
| rs367943980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677894 | CCAGGAAGTCCCCAC[A/G]TTAGCCTCCCTCCCA | 4215 |
| rs368096233 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694436 | CCCAGGCAGGGGCCC[A/G]CGATGTGGAACTGCT | 4215 |
| rs368172093 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681195 | GAGAAGCCTGCCTTT[C/T]GATCCTGGCCAGACC | 4215 |
| rs368232481 | snp | C/G/T | 8.24444e-05 | 0.00642002 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691189 | GGCTGTCTGCGGGAC[C/G/T]GCGCTGAGAAGACCC | 4215 |
| rs368234944 | in-del | -/G | 0.445592 | 0.155704 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649449 | AAAAAAAAAAAAAAA[-/G]TAGACAGGATCTCTG | 4215 |
| rs368260411 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659116 | AGCTCAAATGATCCA[C/T]CCACTTTAGCCTTGC | 4215 |
| rs368267156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628071 | CCACCACGCCCAGCT[A/G]ATTTTTGTATTTTTA | 4215 |
| rs368352492 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671000 | ATTTTGAAAAGATTG[A/G/T]TCTGGCTACAGTGTG | 4215 |
| rs368376876 | snp | C/T | 3.32474e-05 | 0.00407708 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692340 | TCGGGGACGGGCATG[C/T]GCTCCGTCACTGGCA | 4215 |
| rs368406258 | snp | A/G | 6.60012e-05 | 0.00574423 | intron-variant, synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634759 | CAGCCCCACAGTAAC[A/G]ACAAGCTCATGTGCA | 4215 |
| rs368411431 | snp | C/T | 1.65045e-05 | 0.00287263 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691152 | AAAGAACTTGCAGCA[C/T]GAGCGCATCGTGCAG | 4215 |
| rs368550331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627895 | GGCCTGTCACTCTTA[C/T]TTTCTTCAATCCTTT | 4215 |
| rs368584484 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668271 | GAGTTACAGGAAAAA[C/T]ATGTTTCTGAGGTAC | 4215 |
| rs368655819 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662815 | GGCGTGCGCCACTAC[A/G]CCCGGTTAATTTTTG | 4215 |
| rs368661141 | snp | G/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689406 | GATGGGCTGGAGCTG[G/T]TATTATCTATCACTT | 4215 |
| rs368678801 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666920 | AGATGTAGCTTGGCC[C/T]TTTTCCTCTTCTTTT | 4215 |
| rs368687736 | snp | A/T | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681166 | GCCAGGAAGTGTGGG[A/T]GTGGGTAGGAATGGA | 4215 |
| rs368762663 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642427 | CACTTTGGGAGGCCA[A/G]GGCGGGTGGATCACT | 4215 |
| rs368762995 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696750 | TGCTTAACCGAACCA[A/G]GATGATCCTTGCCAT | 4215 |
| rs368785473 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654336 | CGTGACCTTTTTTGT[C/T]TGGCTTCTTTGACTA | 4215 |
| rs368824006 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645780 | CTAGAAACAGCATGT[A/C]ACAGCATAGCAACTG | 4215 |
| rs368830278 | snp | C/G | 1.66313e-05 | 0.00288364 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688503 | AGTGTGCGGGAGTCT[C/G]TTTTTTCTTTTTGTT | 4215 |
| rs368843929 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668987 | AGCATCAAGTAGAGA[C/G]AGATATCTCAGGCAT | 4215 |
| rs368864181 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649419 | CCTAGGCGACAGAGC[A/G]AGACTCCATCTCAAA | 4215 |
| rs368873892 | snp | A/G | 0.000280133 | 0.0118316 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688843 | GAACCTACCCCCGGC[A/G]CTACCACGTGTCTGT | 4215 |
| rs368884539 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660416 | CAGGGTCTTGCCATG[G/T]TGCCCAAGCTGGTCT | 4215 |
| rs369020805 | snp | C/T | 0.000297152 | 0.0121856 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691237 | TACATGCCAGGGGTA[C/T]GTGCCCCTTGAATGC | 4215 |
| rs369110211 | snp | C/T | 1.68556e-05 | 0.00290302 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634666 | CAAACTTATGTTGCA[C/T]GAAGGATACAAATTA | 4215 |
| rs369127053 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637585 | TTATGTCACTTCTTA[C/T]GTTCTGGCACTGCAG | 4215 |
| rs369141732 | snp | C/T | 3.30486e-05 | 0.00406487 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690394 | CCAATTTGATCCAGA[C/T]AGTCCTGAGACAAGC | 4215 |
| rs369189010 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664017 | GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG | 4215 |
| rs369226035 | in-del | -/GAGAG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650692 | AGAGAGAGAGAGAGA[-/GAGAG]TTTTTTTTTTTTTTA | 4215 |
| rs369281595 | snp | A/G | 0.000118472 | 0.00769559 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646103 | CTGATGAGTAGCTGT[A/G]TTCATGTATGCCAAA | 4215 |
| rs369305057 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655288 | TGGGATAACCACCCC[C/T]GTGATTCAGTTACCT | 4215 |
| rs369386987 | snp | A/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620913 | TGAGAGGCTGAAGCA[A/G]GAGAATTGCTTGAAC | 4215 |
| rs369408320 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691932 | TGAGTGCCTGCAGGG[A/G]CCAATCACTTAACCA | 4215 |
| rs369418988 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655249 | TCTCGTGAGAACTCA[C/T]TCACTATCAGGAGAA | 4215 |
| rs369463266 | snp | A/G | 5.13897e-05 | 0.00506875 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693802 | GCCACACAGCTGCCG[A/G]TCGCCCTTTGCTGCA | 4215 |
| rs369465183 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685573 | AAGCTGCCAATCCTT[A/G]GACAGGTCAGCAGAC | 4215 |
| rs369477151 | snp | C/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674944 | AGCAGTGCTCAGGAC[C/G]AGCTTCCAGTCCTAG | 4215 |
| rs369478172 | in-del | -/CCT | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677475 | ACTTAGGAAAACCAT[-/CCT]TTTTTTACAGTTGCA | 4215 |
| rs369518145 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639821 | ATGATTATAAAGCAA[C/T]CTTCTTACAAAATAT | 4215 |
| rs369531094 | snp | C/T | 1.64958e-05 | 0.00287187 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691842 | TGCACAGCAACATGA[C/T]TGTTCACCGGGACAT | 4215 |
| rs369597285 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638181 | CCACTGATCTCCTAC[A/C]ACTTTCCAGAGTCAT | 4215 |
| rs369611006 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667772 | ATTTGTATTTTTTTG[C/T]TATTGTTATTTTTTA | 4215 |
| rs369632918 | snp | C/G/T | 3.31539e-05 | 0.00407137 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693508 | GGACAGCTGGGAGTC[C/G/T]AGGGCTGGCTGAGGG | 4215 |
| rs369713016 | snp | A/G | 0.000183143 | 0.00956756 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681949 | TGTATCAGCAGACCA[A/G]GCTCATAACAAGGGG | 4215 |
| rs369727274 | snp | C/T | 3.31669e-05 | 0.00407215 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691728 | TGACTTCTTGTGGCC[C/T]CCAGGGCTCGGTGAA | 4215 |
| rs369853997 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678898 | AGCTGGGTATGGTGA[C/T]GGCCACCTGTAATCC | 4215 |
| rs369867601 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669915 | TGAGACTAGCCTGGG[C/T]AACATGGCAAAACCC | 4215 |
| rs369869258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692633 | GGGAACTTAGGCCAT[A/G]GAAAACATCCCTCAT | 4215 |
| rs369939128 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673635 | GGACTTGTCGGCGGG[A/G]TGCAGTGGCTCATGC | 4215 |
| rs369943434 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647551 | AGCTGCCAGATTGAA[A/C]CCACAAATATTTAAG | 4215 |
| rs370051005 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646791 | AAGTTATTTAAGGAA[A/G]ACATTCAGAAAGCAT | 4215 |
| rs370167226 | snp | C/T | 0.029116 | 0.117091 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660677 | GGCTCACCGCAACCT[C/T]TGGCTTCCAGGTTCA | 4215 |
| rs370207376 | snp | C/T | 5.44104e-05 | 0.00521558 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689567 | ACATTTCCCCGAATA[C/T]GGCGTCATCAAGGCA | 4215 |
| rs370211518 | snp | C/T | 0.000132065 | 0.00812498 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632682 | CTCTTTCATTGCAGA[C/T]GAACAGGAGGCATTG | 4215 |
| rs370216632 | snp | A/G | 3.30978e-05 | 0.0040679 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692219 | GGGTCCAGGGTTGCA[A/G]CCTCTGCCCTTTCAT | 4215 |
| rs370255751 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641444 | GACGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 4215 |
| rs370290125 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648845 | AGAATTACAGTCTCA[A/G]TGGGTTTCCTAGTGG | 4215 |
| rs370304509 | snp | A/G | 1.71234e-05 | 0.00292599 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691081 | CCTGAGAGCTGAGGC[A/G]ACCACTGACCCCTCC | 4215 |
| rs370361220 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681434 | GAAGAGAGAAGGTGA[C/T]ATTATGAAGGAGTAA | 4215 |
| rs370379512 | snp | A/T | 1.74048e-05 | 0.00294993 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691075 | TAGGGCCCTGAGAGC[A/T]GAGGCGACCACTGAC | 4215 |
| rs370385618 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654315 | GTGTAGTGCAATCAT[A/C]CAGTACGTGACCTTT | 4215 |
| rs370404986 | snp | C/T | 2.02792e-05 | 0.00318421 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657761 | TAAACTTCTGTTTTA[C/T]ATTATTTTCCTTTTC | 4215 |
| rs370434140 | snp | C/T | 0.000166008 | 0.00910915 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691881 | AGCAGGGCCAGGATA[C/T]ATGGAGTCCCCAGGA | 4215 |
| rs370467423 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662346 | CCTGAGGCCGGGAGG[C/T]TGAGGCCGCAGTGAG | 4215 |
| rs370488541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628106 | TGATGAGGTTTCACC[A/G]TGTTGACCAGGCTGG | 4215 |
| rs370542508 | snp | C/T | 6.6846e-05 | 0.00578088 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690425 | AAGGTACACTTAACC[C/T]GTGGTCTGACTTCAG | 4215 |
| rs370582811 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639137 | TATGACTATGCCTCA[C/T]TGTGTGGTACAGAGA | 4215 |
| rs370618710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661873 | CTTTGGGAGGCCGAG[A/G]CAGGCGGATCACAAG | 4215 |
| rs370621293 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640330 | GGGAGACTAGTTTAG[A/G]AGAGTAGTTGATATA | 4215 |
| rs370624784 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630707 | TATGTGTTAATTTGA[C/T]AGATGTCTTTTTGTA | 4215 |
| rs370632620 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695150 | GGGAGCTGGGGATTA[C/G]TGCCAGGCAGCCCTG | 4215 |
| rs370717303 | snp | C/T | 1.64852e-05 | 0.00287094 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688858 | GCTACCACGTGTCTG[C/T]GCACCACAAGGACTA | 4215 |
| rs370737338 | in-del | -/A/AA/AAA | 0.312593 | 0.242037 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687210 | TCTCTACTAAAAATG[-/A/AA/AAA]AAAAAAAAAAAAAAG | 4215 |
| rs370742358 | snp | A/C | 1.65384e-05 | 0.00287557 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632660 | TAAGTGTCTTAGTCC[A/C]TGTGCTCTCTTTCAT | 4215 |
| rs370749424 | snp | G/T | 3.334e-05 | 0.00408276 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690419 | ACAAGCAAGGTACAC[G/T]TAACCCGTGGTCTGA | 4215 |
| rs370750559 | in-del | -/TC | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690256 | TCTTTCCTTCTGCTC[-/TC]CTGTAGCTCCCAGTG | 4215 |
| rs370846676 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656378 | TAGGCTGAGGTGGGC[A/T]GATTACTTGAGGTCA | 4215 |
| rs370948187 | snp | C/G | 6.8725e-05 | 0.00586155 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652535 | ATACAATTAACCAAC[C/G]TTTCTTTCTGTTTCT | 4215 |
| rs371150816 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638030 | CTTTCAGTGTGAAAG[-/A]CCTGGCTCTTCAGGA | 4215 |
| rs371194292 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688792 | TGTCTTACTCAGATC[A/G]GGAAACTCAGCTTTA | 4215 |
| rs371209476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670373 | GGATTGCTTGAGGCC[A/G]GGAGTTTGAGACCAG | 4215 |
| rs371230077 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647165 | ATTCACAAGCCTACA[A/G]GGTTGTCAGAGGCAA | 4215 |
| rs371429490 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677312 | CTTCTGCTGCTGACA[A/G]ATGTTGCTGACATGT | 4215 |
| rs371448720 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664196 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 4215 |
| rs371490556 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668858 | TGGGCTGAGATGAAT[C/G]CTGCAGTGAAGCATT | 4215 |
| rs371515350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651913 | CATCTCAAAGATGAA[C/T]GATGGAAAAGACCTT | 4215 |
| rs371537958 | snp | A/G/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679693 | ATGTTGCCCATGCTG[A/G/T]TCTCAAACTCCTGGC | 4215 |
| rs371569098 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678281 | CTTGACTGATTTTAT[C/T]GCTCTGTTAGTTCAT | 4215 |
| rs371576369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652981 | TCTTATTTTTTTCCC[A/C]CCAGCACAGCCTTAA | 4215 |
| rs371639415 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660597 | TCTTCTTCTTTTCTT[C/T]TTTTTTTTATTTGAG | 4215 |
| rs371824483 | snp | G/T | 7.56516e-05 | 0.0061498 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689506 | GCCTCGTAGCCTGGG[G/T]TGTGACTTGCTCTCC | 4215 |
| rs371837391 | snp | A/G | 4.94662e-05 | 0.00497299 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691190 | GCTGTCTGCGGGACC[A/G]CGCTGAGAAGACCCT | 4215 |
| rs371842398 | snp | C/T | 5.41785e-05 | 0.00520445 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681751 | GTTGTTGAAAGCCTC[C/T]TTTATGTGCTCTAGG | 4215 |
| rs371965403 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666954 | GAACAGTTCCTCTCC[C/T]CACTCTGGGGTGTCC | 4215 |
| rs372085589 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687852 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGCGAG | 4215 |
| rs372091631 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659851 | TCTTTTTTTAAATAC[A/G]AAAACTGAGAAGTGA | 4215 |
| rs372155467 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648156 | CTGTTATTCAATAGG[A/G]TGGCAGCAGCTTAGA | 4215 |
| rs372179093 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689667 | AATACCTGGACCCCC[A/G]TGGGCGCCTGCGGAG | 4215 |
| rs372206804 | snp | C/G | 6.66744e-05 | 0.00577345 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63646037 | TCTTTTTGGCAGAGT[C/G]ACGTCAGAATCAAGT | 4215 |
| rs372241747 | in-del | C/GT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662856 | GGAGATGGGGTTGGG[C/GT]GGGGGGCGGTCCTCA | 4215 |
| rs372254945 | snp | A/T | 1.72698e-05 | 0.00293847 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690214 | GAGAATGAATGGGAT[A/T]TTCATAAATAATGTA | 4215 |
| rs372297810 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663802 | GAGGCTGAGGCGGGA[A/G]GATCACTTGAGCCAA | 4215 |
| rs372303956 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636742 | GACAATGACATTGAC[C/T]TGTTTGTCAGCGACA | 4215 |
| rs372305089 | snp | A/G | 0.000116356 | 0.00762655 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692445 | GGACATGCAGAACCC[A/G]TTCTTCCACCCAGGC | 4215 |
| rs372317011 | snp | G/T | 0 | 0 | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696339 | AGTGCTTTCAGTTGT[G/T]GGGGGTGGAGGTAGG | 4215 |
| rs372318865 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634658 | AATGTTGTCAAACTT[A/G]TGTTGCACGAAGGAT | 4215 |
| rs372339060 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655022 | AGAGTTGAGACTCTG[C/T]CTCAAAAAACGATTA | 4215 |
| rs372344776 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653452 | ATGAGGAGTTAAAAT[G/T]TTTCTTTTAGTAAAG | 4215 |
| rs372374104 | snp | C/T | 0.000349733 | 0.0132191 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692456 | ACCCATTCTTCCACC[C/T]AGGCCATAGTGGCCC | 4215 |
| rs372390229 | snp | A/G | 1.72169e-05 | 0.00293396 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689636 | ACAAATGGCGAGAAC[A/G]TGGGTCTGGCTGTGC | 4215 |
| rs372455415 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631583 | TCTCCAAATGCTATT[C/T]GAATGGGCAAAGATC | 4215 |
| rs372467635 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660285 | AGCTCACCACAGCCT[C/G]AACCTCCCAGACTCA | 4215 |
| rs372472600 | snp | A/G | 6.59739e-05 | 0.00574305 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691167 | TGAGCGCATCGTGCA[A/G]TACTATGGCTGTCTG | 4215 |
| rs372488037 | snp | A/C/T | 0.000619498 | 0.017589 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646122 | ATGTATGCCAAAGTT[A/C/T]TCAGATAGCATTGAG | 4215 |
| rs372510401 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628830 | GTAATAAAATTAAGT[A/T]TTAGGGTAGATTAAA | 4215 |
| rs372513019 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629110 | CTAACTGCTTCAGTC[G/T]AAGAAAGTTGTTATT | 4215 |
| rs372612179 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638035 | GTGTGAAAGACCTGG[-/CT]CTCTTCAGGACCTCC | 4215 |
| rs372811612 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628409 | CTTGTTGCCCAGGCT[A/G]GAGTGCAATGGCACC | 4215 |
| rs372841169 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661978 | CGTGGTGGCAGGTGC[C/T]TGTAGTCCCAGCTAC | 4215 |
| rs372850028 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631312 | GTCAATCAGTTAATC[A/G]GTAGTGGGAGAAGAG | 4215 |
| rs372854096 | snp | A/C | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683246 | GAAGCCCTTTGTACT[A/C]TTCTTCCTTCTATAC | 4215 |
| rs372868343 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645400 | CTGGGAACAGTGTAT[A/G]AGATCCTACTTTACC | 4215 |
| rs372885872 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648784 | CGAGCCACTGCACTC[C/T]AGCCTGGGGGACAGA | 4215 |
| rs372906669 | snp | G/T | 0.000158628 | 0.00890443 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691071 | GAACTAGGGCCCTGA[G/T]AGCTGAGGCGACCAC | 4215 |
| rs372986161 | snp | C/G | 1.65831e-05 | 0.00287945 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691876 | GGGTGAGCAGGGCCA[C/G]GATACATGGAGTCCC | 4215 |
| rs372995382 | snp | A/C/T | 0.000159724 | 0.00893534 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691050 | TGAGCTGAACCCAGG[A/C/T]GGGCAGAACTAGGGC | 4215 |
| rs373013552 | snp | C/G | 3.31636e-05 | 0.00407194 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688641 | AGGGTGTCTGGGTGG[C/G]GCCTCAGGTGGCTCT | 4215 |
| rs373025363 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638564 | TGAATCTGTAGCTCA[A/G]CCCGACAGCCCGCAC | 4215 |
| rs373116535 | snp | C/G | 1.70455e-05 | 0.00291933 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690242 | GTACACAAAGTAACT[C/G]TTTCCTTCTGCTCTC | 4215 |
| rs373165655 | in-del | -/CAAA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629584 | GAAAAAAAACAAAAA[-/CAAA]ACCTCAATCCAGGAA | 4215 |
| rs373172363 | snp | A/G | 7.24769e-05 | 0.0060194 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681909 | CAGTGCGTGAGTATA[A/G]GGGGGCTGGGATATG | 4215 |
| rs373212876 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679547 | GAGTGCAGTGGTCCA[A/G]ACACGGCTCACTGCG | 4215 |
| rs373234686 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683747 | CTGAAAAGTGAAAAT[A/G]TGATAAGTTTTGTTT | 4215 |
| rs373235108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659617 | GGCTCACTGCAACCT[C/T]CACCTCCCGGGTTCA | 4215 |
| rs373241095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666781 | GTGGTTTGCTGAGAC[A/G]AATAGAAGAGTGAGA | 4215 |
| rs373265314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647266 | CCTGGAGGGAGGAAG[C/G]TCTGAGCTCTGTCCC | 4215 |
| rs373316092 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655617 | CACCTCAGTTTCCCC[A/G]GTAACTGGGACAATA | 4215 |
| rs373380834 | snp | C/T | 0.000115472 | 0.00759756 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691762 | CCAGTTGAAGGCTTA[C/T]GGTGCTCTGACAGAG | 4215 |
| rs373382603 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652664 | ACAATGAGGTGAGAA[A/G]GCAGATGGATGGGGC | 4215 |
| rs373395780 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676378 | AGGGGGACCATGGAT[A/G]TTTTATCCCAGGGAA | 4215 |
| rs373408046 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649470 | AGGATCTCTGTTGCT[C/G]AGGCTGGAGTACAGT | 4215 |
| rs373504394 | snp | C/T | 3.30836e-05 | 0.00406702 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693541 | GACACGGGGTTCTCT[C/T]TTTCCAGGAGCCTGG | 4215 |
| rs373679160 | snp | A/G | 5.00822e-05 | 0.00500386 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693778 | CAGCTCATGTACTGA[A/G]CTCTCACGGCCACAC | 4215 |
| rs373701745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656538 | TGAACCCAGGAGGTG[C/G]ACATTGCAGCAAGTT | 4215 |
| rs373725130 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656816 | TCACGCTGCTGTAAA[A/C]AACTGCCCAAGACTG | 4215 |
| rs373837691 | snp | A/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691445 | GACAGCTGTCCTAGG[A/T]CCAGCACTCCCCTGA | 4215 |
| rs373851514 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672632 | CAGAGACTATAGAAT[A/G]AGAAGAAAAGAGGGT | 4215 |
| rs373872525 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678477 | GAGACAGGAAATCCA[G/T]CAAAATTCTATGCCT | 4215 |
| rs373940578 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665457 | GGCATGAGCCACTCC[C/T]GGCCTAGCTTTTAGA | 4215 |
| rs373960837 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632632 | TTGTGAAAGAGCTTT[A/G]CTGGTCTGTATTTAA | 4215 |
| rs373977573 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657414 | ATGAATTGTATGAGT[C/G]TAAATGGAATGAAAT | 4215 |
| rs373978655 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623918 | TCCTTTTTGTAGGAG[G/T]TTAACTGTACGCTAT | 4215 |
| rs373979108 | snp | A/G | 1.67556e-05 | 0.0028944 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688487 | GCTTGGTTGCTGTGG[A/G]AGTGTGCGGGAGTCT | 4215 |
| rs374032639 | snp | C/T | 4.9657e-05 | 0.00498257 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688892 | TGATGGTGAGTTCTT[C/T]TTCACCTGCTCCCTG | 4215 |
| rs374045857 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652776 | AGGTTTTCATTTTCT[A/G]GACCCCCTTTTCTTA | 4215 |
| rs374080790 | snp | G/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678822 | ATCACCTGAAGACAA[G/T]AGTTCAAGACCAGCC | 4215 |
| rs374083706 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655175 | ACACATCCTTCACAT[G/T]GCGACAGGAGAGAGA | 4215 |
| rs374113385 | snp | C/T | 8.26631e-05 | 0.00642843 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632665 | GTCTTAGTCCATGTG[C/T]TCTCTTTCATTGCAG | 4215 |
| rs374155171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688468 | GAGACTGCCTGGACG[C/T]CCTGCTTGGTTGCTG | 4215 |
| rs374181670 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632805 | CTCAAATAGGCAGGT[C/G]TGTGTGACCCTGGCA | 4215 |
| rs374254974 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668729 | GGCTGAGAATGCTGA[A/G]GAGTGAGATTTCTGT | 4215 |
| rs374259002 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643187 | ACAAAAAGAAATATA[C/T]CATACTAATGTAAGA | 4215 |
| rs374290897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650096 | GCTTAGGTGTACTAA[A/G]AGATGAAGGTTGTTT | 4215 |
| rs374295158 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663586 | AAAGCGTTTAAGAGC[A/G]TGGATAATGAAGACA | 4215 |
| rs374343505 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628383 | TTTTTTTTTTGAGAC[A/G]GAGTTTCGCTCTTGT | 4215 |
| rs374473399 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682549 | CTGCCTGCCTTTCTT[A/G]AGTTTGAGGCTCTTT | 4215 |
| rs374490049 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642421 | TCCAAGCACTTTGGG[A/G]GGCCAAGGCGGGTGG | 4215 |
| rs374575721 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644840 | GCCTATTAATTTGTC[C/T]TCTTCAAAATAATTT | 4215 |
| rs374633546 | snp | A/G | 1.65203e-05 | 0.002874 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691137 | CGAGATCCAGTTGCT[A/G]AAGAACTTGCAGCAT | 4215 |
| rs374735208 | snp | C/G | 1.65392e-05 | 0.00287564 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657872 | TCAAGCATGAAAAGC[C/G]TTAGGATATTGCTGT | 4215 |
| rs374741318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664563 | GGACTTTTGTAACTT[A/T]TTTTTCTACTGATCT | 4215 |
| rs374801462 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666985 | AGACAGGTGCGGATC[A/G]AGGCTTCCCAGTCCG | 4215 |
| rs374804258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633690 | TCTCACCTGTAGTGC[C/T]ACTTACCTGTTTCCT | 4215 |
| rs374805445 | in-del | -/CT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660939 | CTTCTAATTTTCCTT[-/CT]GTCTTCATTCCTCAC | 4215 |
| rs374807460 | snp | C/G | 1.79271e-05 | 0.00299386 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63681777 | CTAGGCTCCCAGAAC[C/G]CTGGCCGAAGCTCAC | 4215 |
| rs374835082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677854 | AAGAAAGAAAGATAC[A/G]TGGCACTGTGCTTCC | 4215 |
| rs374872710 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695444 | CATGCGCCAGTTGGG[C/T]CTGGACCCTCCTGTG | 4215 |
| rs374885826 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660478 | TCAGCCTCGCAAAGT[A/G]CTGGGATTACAGGTT | 4215 |
| rs374925046 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675531 | AAAGAACCTACCATA[C/T]CCGAGGGTGAGAGTG | 4215 |
| rs374986406 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659827 | GCCACTGTGCCCGGC[C/T]GTACCAGTTCTTTTT | 4215 |
| rs375031748 | snp | C/G | 1.64972e-05 | 0.00287199 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690376 | ACTTGCTTCCAAGCA[C/G]GTCCAATTTGATCCA | 4215 |
| rs375074088 | in-del | -/AGAGAGAG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650659 | CTCTCTGTCTCTTAT[-/AGAGAGAG]AGAGAGAGAGAGAGA | 4215 |
| rs375081825 | snp | G/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694892 | GAGGTCTCAGCCCCT[G/T]TCCCTTGTAGCTCCT | 4215 |
| rs375099706 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637250 | AGTTGTTACTCATCT[A/G]TTAATGTAGGATTTT | 4215 |
| rs375125085 | snp | A/G | 0.000134628 | 0.00820341 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634677 | TGCACGAAGGATACA[A/G]ATTATTAACCTCAGT | 4215 |
| rs375158743 | snp | A/G/T | 8.55507e-05 | 0.00653983 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693801 | GGCCACACAGCTGCC[A/G/T]GTCGCCCTTTGCTGC | 4215 |
| rs375250733 | snp | C/T | 8.32702e-05 | 0.00645199 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63646063 | CAAGTTCGAGCACAA[C/T]GGGGAGAGGCGGTAA | 4215 |
| rs375274233 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665465 | CCACTCCCGGCCTAG[C/G]TTTTAGATTTTTTAA | 4215 |
| rs375288012 | snp | G/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683546 | AGGATTTGACTCCCA[G/T]TGAGGACAGACTTTT | 4215 |
| rs375347371 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691659 | CCTTTGCTGCCATGC[C/T]GGGGGCTGGAATGGG | 4215 |
| rs375361455 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643075 | AAACTTCTAAAAATG[A/G]AAAAAAAAAAAAATT | 4215 |
| rs375396310 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692465 | TCCACCCAGGCCATA[A/G]TGGCCCCCCATTAGA | 4215 |
| rs375404985 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693513 | GCTGGGAGTCCAGGG[A/C]TGGCTGAGGGGTGAC | 4215 |
| rs375435691 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667836 | TGAATCCACAGATGC[A/G]GAACCTGGAGATATG | 4215 |
| rs375460285 | snp | C/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672939 | GAGAGACTTGGAAAA[C/G]TCCTAGCAGTAGAAA | 4215 |
| rs375481266 | snp | C/T | 1.67089e-05 | 0.00289035 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691698 | TCCACCAGCCCTCCC[C/T]TGAGGGGACTCCTCT | 4215 |
| rs375649402 | in-del | -/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682603 | GAATTCAGTTTTTTT[-/T]GTGGCTGTAGGACTG | 4215 |
| rs375687375 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648671 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCCGG | 4215 |
| rs375719334 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678701 | ACCACATGAACCATA[C/T]GTTCTGAACAACTGA | 4215 |
| rs375767884 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670516 | TGAACCTGAGAGATC[A/G]AGGCTGCAGTGAGTG | 4215 |
| rs375813340 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629012 | ATCTCCATTTTACAG[A/T]TGAGGAAATTGAGGT | 4215 |
| rs375846071 | snp | G/T | 4.89668e-05 | 0.00494783 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689515 | CCTGGGGTGTGACTT[G/T]CTCTCCTCTGGCCCT | 4215 |
| rs375871340 | snp | A/T | 0.00015824 | 0.00889354 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691072 | AACTAGGGCCCTGAG[A/T]GCTGAGGCGACCACT | 4215 |
| rs375880648 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662263 | AAAAAAAAAAAAAAA[C/T]GAAAATTAGCCAGGT | 4215 |
| rs375968852 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665173 | GCTGGGCGTGGTGGC[A/G]CATGCCTGTAATCCC | 4215 |
| rs376043954 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666901 | GATAGGCCTGACTGT[A/G]TAAAGATGTAGCTTG | 4215 |
| rs376081084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677824 | AGTGAGCTATGAACA[C/T]GCCACTGCACTCCAA | 4215 |
| rs376092350 | snp | A/G | 9.89283e-05 | 0.00703238 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691192 | TGTCTGCGGGACCGC[A/G]CTGAGAAGACCCTGA | 4215 |
| rs376168432 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656859 | AGGAAAGAGGTTTAA[C/T]TGACTCACAGTTCAG | 4215 |
| rs376179728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667454 | ACCTCTTGCTTATGA[C/T]TCCTGAGAAGTCTTT | 4215 |
| rs376276125 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644374 | TGTGCGCCATTACTC[-/A]CGGCACACTTTTTGT | 4215 |
| rs376304594 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661642 | TGTTACCTCATATTC[C/G]CGTTGACAAAAATAA | 4215 |
| rs376358910 | snp | G/T | 0.000247105 | 0.0111127 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652690 | GGGGCAGGGACAAGA[G/T]GGGCAGATGCCTACC | 4215 |
| rs376414848 | snp | A/C | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676013 | ATGAAGATTAAAAAC[A/C]AAACTGAAAATGCCC | 4215 |
| rs376421668 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679632 | GGTCCACAAGTGTGC[A/G]CCTGGCTAATTTTTA | 4215 |
| rs376570118 | snp | C/T | 3.30453e-05 | 0.00406467 | synonymous-codon, missense | MAP3K3 | GRCh38.p7 | 17:63693564 | GAGCCTGGGCTGCAC[C/T]GTGGTGGAGATGCTG | 4215 |
| rs376633157 | snp | A/G/T | 0.00016505 | 0.00908294 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632837 | AGCTAAGTGAGATTT[A/G/T]TTGGGGAGGGGTTTT | 4215 |
| rs376662686 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682196 | CAGGCAGGCACCACC[A/G]CGCCCAGCTCATTTC | 4215 |
| rs376718918 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660206 | ACCTATTCCTTTATT[C/T]CCCTTTTTTTTTGAG | 4215 |
| rs376726068 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628198 | GGTGTGAGCCACCAC[A/G]CCCAGCCAGCTTGCT | 4215 |
| rs376726883 | snp | C/G/T | 4.09679e-05 | 0.00452577 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689731 | GAGGAATGTGCCAAC[C/G/T]AAGTGTGAGGAGCTG | 4215 |
| rs376757225 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629582 | AGGAAAAAAAACAAA[A/C]ACAAAACCTCAATCC | 4215 |
| rs376767672 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689983 | CCCTTCATCCCTGCC[A/G]TATTAAGATATTTAG | 4215 |
| rs376776007 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664914 | CCATTCCCTTTTGCC[C/T]CCTTAAATTGAGGTT | 4215 |
| rs376817593 | snp | A/T | 0.00058328 | 0.0170675 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688498 | GTGGAAGTGTGCGGG[A/T]GTCTGTTTTTTCTTT | 4215 |
| rs376852751 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625340 | TGGGATTGACTGGTT[A/G]TTTTTTCTTGGTCAC | 4215 |
| rs376855532 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655448 | TATTTTCTTCTTTTA[A/G]TAGCCATCCTAGTAG | 4215 |
| rs376890092 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683068 | AACTTGCTTTGATGT[A/G]AAAGAAAAGGCTGCT | 4215 |
| rs377003394 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691173 | CATCGTGCAGTACTA[C/T]GGCTGTCTGCGGGAC | 4215 |
| rs377007294 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668667 | ATACTTAGCCACTGG[A/G]CCCTTTCTCCATGTT | 4215 |
| rs377080110 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684809 | ATGTAATGTTTAATG[C/T]TGGAGCTCGGATAAT | 4215 |
| rs377122391 | in-del | -/A | 0.330249 | 0.23677 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687350 | TCTACTAAAAAATAC[-/A]AAAAAAAAAAAAAAT | 4215 |
| rs377239859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665458 | GCATGAGCCACTCCC[A/G]GCCTAGCTTTTAGAT | 4215 |
| rs377263041 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660801 | GAGTTTCTCCATGTT[A/G]GTCAGGCTGGTCTTG | 4215 |
| rs377279069 | snp | A/C | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683774 | GTTTTTTCTTTAATC[A/C]GGTTTAAGCAATAAT | 4215 |
| rs377309387 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639102 | GGAAGTGAGGACTAC[A/G]TGAAAAAAAGAAAGT | 4215 |
| rs377324109 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641093 | TATTACCATTTACCA[A/G]CCACTTGTATATCAG | 4215 |
| rs377337270 | snp | C/T | | | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695619 | CGGCCTCTCTACGAC[C/T]CCATCTTGGTGGCTG | 4215 |
| rs377363072 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676899 | GAAGCCTGTTAATCT[C/T]ATAGAAGTGCATGTG | 4215 |
| rs377534151 | snp | G/T | 3.2963e-05 | 0.00405961 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688778 | GCCAGTGATTCCCCT[G/T]TCTTACTCAGATCGG | 4215 |
| rs377609877 | snp | C/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670491 | AGGGGGCTGAGGCAG[C/G]AGGATCACTTGAACC | 4215 |
| rs377701797 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642029 | TGAATCAAATTATCT[C/T]TATCTGAACTTCCCT | 4215 |
| rs377741494 | snp | A/G | 1.69991e-05 | 0.00291535 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657927 | GTAGCCCTTGTCATG[A/G]TCTGGCAGCTGAAGA | 4215 |
| rs386798303 | multinucleotide-polymorphism | AAG/TAC | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677851 | CCAAAGAAAGAAAGA[AAG/TAC]ATGGCACTGTGCTTC | 4215 |
| rs397756821 | in-del | -/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671274 | CTTTTTTTTTTTTTT[-/T]GTGACGGAGTCTTGC | 4215 |
| rs397777278 | in-del | -/A | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673415 | AACAAACAAAAAAAA[-/A]CCCTACTAAGTAATG | 4215 |
| rs397857822 | in-del | -/A | 0 | 0 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675272 | TTGAGAAAGAAAAAA[-/A]GTTTGATTTCTCTCC | 4215 |
| rs397959129 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645313 | TCTCAAAAAAAAAAA[-/A]GAAACATGATAGACC | 4215 |
| rs527255957 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674963 | TTCCAGTCCTAGTAC[C/T]GATTTGAAAGGGTAG | 4215 |
| rs527268764 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638734 | TGTGCCTATGGTCAC[A/G]CTTCTCAGACACACA | 4215 |
| rs527311495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637077 | AGTTTGAGAGCGTGT[A/G]TAGAGTGTCGATGTT | 4215 |
| rs527373559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644976 | CTCTCCTTTCCCTGT[A/C]ATTTTTTAAACTCCC | 4215 |
| rs527565829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659980 | TTTTCAAAGGGCCCT[C/T]TCCATTTCTTTACTT | 4215 |
| rs527634423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646885 | CATAAATGTGCCTTT[C/T]GGTGTTTTTTCCACT | 4215 |
| rs527642426 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655015 | TTGAGACAGAGTTGA[A/G]ACTCTGTCTCAAAAA | 4215 |
| rs527700167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654361 | TGACTAAGCGTATGT[C/T]TTCAACGGTCATCTG | 4215 |
| rs527767833 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669370 | GCCTGGGTGTTTTCT[A/C]AGGGACTCTCAGCTG | 4215 |
| rs527768475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662064 | GCCAGGATTGCGCCA[C/T]TGCACTCCAGCCTGA | 4215 |
| rs527851837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624674 | GAAGACACATGTAAA[A/C]GGAACATGCAAGAGG | 4215 |
| rs527893724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667700 | AGTTTAAATCATCTC[C/T]GGGTTATTTATAATA | 4215 |
| rs527894166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675731 | TTTGCTTCAGCTGGT[A/G]GCACAGGTGGCGCAG | 4215 |
| rs527915020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623865 | CCCCATGTGAAGAGG[C/G]AGCCTTAATGTTTGC | 4215 |
| rs527959745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683258 | ACTCTTCTTCCTTCT[A/G]TACTCCTGCCTTCCA | 4215 |
| rs527973889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631254 | GATTGCACCACTGCA[C/T]TCTAGCCTGGGCAAC | 4215 |
| rs527981203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638494 | CCAGACTTTGAGAAG[A/G]TCATTTCTGCTTTAG | 4215 |
| rs528028703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682609 | CAGTTTTTTTGTGGC[C/T]GTAGGACTGTGGTTC | 4215 |
| rs528087626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670348 | AGCACTTGGTGAGGC[C/T]GAGGTGAGTGGATTG | 4215 |
| rs528194590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633082 | AAAAACACAAAATTA[A/G]CCAGGTGTGGTGGTC | 4215 |
| rs528208466 | snp | C/G | 0.0138799 | 0.0821421 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621931 | ACTGCGCCAGCCCGC[C/G]CGCCCGCCGAGCCTT | 4215 |
| rs528235686 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626306 | AGAAGTTACAGTTAG[A/G]TAAGGTGAAGCAGAA | 4215 |
| rs528239609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639912 | TAAAGATATAATGCT[G/T]TATATCTTATTGACT | 4215 |
| rs528283853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693430 | CTGAGGTATCCCTCA[C/G]CTTGGCCTGTCCTGC | 4215 |
| rs528301840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639290 | CGGAGGAAGGGTGGC[A/C]CTCCAGGTCAGGAAA | 4215 |
| rs528331950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692936 | GGCCTTTGCAGATAG[A/G]ATTAGGTTAAGGGTT | 4215 |
| rs528419801 | in-del | -/AAAC | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651475 | CGAGACTCTGTTTTG[-/AAAC]AAACAAACAAAAAAA | 4215 |
| rs528506457 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632179 | CTGCAGGAAATCTGA[C/T]TGGAGGGCTATTAAG | 4215 |
| rs528523414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641840 | ATGGTCATGTGTTTG[A/G]GGAGGGGTGGGAGAG | 4215 |
| rs528705722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656813 | TTCTCACGCTGCTGT[A/G]AAAAACTGCCCAAGA | 4215 |
| rs528718116 | snp | A/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677292 | CACTTACCTCCTTAG[A/T]GTTGCTTCTGCTGCT | 4215 |
| rs528807512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671303 | GCTCTGTCACCAGGC[C/T]GAAGTGCAGTGGTGT | 4215 |
| rs528831435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663356 | GAAAATACAAAATTA[C/G]CTGAGCGTGGTGGCG | 4215 |
| rs528869918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625632 | AGAATAGTCTCAATT[C/G]AGTTTGGCTAGAATC | 4215 |
| rs528909231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684293 | TTTGGTATTCTTCCT[C/T]CACCACACCTGCCAT | 4215 |
| rs528932989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632530 | AATTCAAATTGCCAT[A/G]GTCTGACCTTTTGGG | 4215 |
| rs528982316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639207 | TGGGCCAGAGGAGCT[A/G]TGGAGTCATTTCAGG | 4215 |
| rs528999190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692777 | ACTTGCTCGACATAA[C/T]CTTGTGTCTATCCTC | 4215 |
| rs529037723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638677 | TGAATTTCTGTACTA[C/G]AACTTTTTTCTCAGT | 4215 |
| rs529098963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646792 | AGTTATTTAAGGAAA[A/G]CATTCAGAAAGCATA | 4215 |
| rs529130287 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654299 | CTATTCTGAACATTT[C/T]GTGTAGTGCAATCAT | 4215 |
| rs529191725 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662034 | CATGAACCCAGGAGG[A/C/T]GGAGCTTGCAGTGAG | 4215 |
| rs529195838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653569 | TATAAATCATTGTTA[C/T]TATTTTAGTTCATAC | 4215 |
| rs529247036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641201 | ACTTTACAGATGAGG[A/T]AACTAAGTTATAGGT | 4215 |
| rs529285779 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694102 | CACTGCAATTGGCAC[C/T]GAAGCCCAGAGGGTC | 4215 |
| rs529325618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649193 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 4215 |
| rs529389186 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648644 | ATATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 4215 |
| rs529450682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656240 | GTCTCAAAAAAAAAA[A/G]TCTTGTATTATAAAT | 4215 |
| rs529496012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663192 | GGAGTCACTTTCATA[C/T]ATGAACAGTGTAAAA | 4215 |
| rs529571459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677236 | CTGATCTGAACCCAC[A/G]TATATCTAATTTCAA | 4215 |
| rs529624807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626198 | TTTTTCTGGTTCTAT[A/G]GAAGCTGTTAATTTA | 4215 |
| rs529662727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665165 | AAAAATTAGCTGGGC[G/T]TGGTGGCACATGCCT | 4215 |
| rs529665176 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671513 | CCTGCCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 4215 |
| rs529771113 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629620 | AATGCCTAAAAGAGC[C/T]ACTTGATTTACTTCC | 4215 |
| rs529843441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671595 | AAGACATGACACTCA[A/G]TTCTCTCACAAGGGT | 4215 |
| rs529854710 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682799 | CACATAATCATAGGA[A/G]TGAATATTCTATCCT | 4215 |
| rs529856531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671335 | ATCTCGGCTCACTGC[A/G]ACCTCCGCCTCCCGG | 4215 |
| rs529875303 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650375 | GGTGTGATCTCAGCT[C/G]ACTGCAACCTCTGCC | 4215 |
| rs529924643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678961 | TTGAACCCAGGAGGC[A/G]GAGGTTGCCTTGAGC | 4215 |
| rs529937926 | snp | C/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620950 | GACGGAGGTTGCAGT[C/G]AGCCGAGATCGCGCC | 4215 |
| rs529988004 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678265 | AAGAAAAAAAAATTG[C/G]CTTGACTGATTTTAT | 4215 |
| rs529989994 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687506 | AACAGTGTGAGATTC[C/T]GTCTCAAAAAGAAAA | 4215 |
| rs529995074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634121 | GGGCCCATTCTTACA[C/G]TATTTTCATATGTTA | 4215 |
| rs530020040 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659038 | ACTGTGCCCGGCCAT[G/T]TTTTAATTTTTTTAG | 4215 |
| rs530052125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686525 | AGGGATTGACTCTGG[C/T]TTTGGATTATCTCCT | 4215 |
| rs530089039 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621632 | GAGGTGTGAGACAGG[G/T]AAAGCTGGGCTGGGC | 4215 |
| rs530133786 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636610 | CTGTGGCTGAACATG[C/T]TGGAGAAGAGCTTGC | 4215 |
| rs530165210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679739 | TGCCTCTCGAAGTGT[C/T]GGGATAATAGGTGTG | 4215 |
| rs530190816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643466 | CAGTGAGCCGTGATC[A/G]TACCACTGCACTCCA | 4215 |
| rs530203202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667286 | GATATAGTAGTGTGA[C/T]TAAATTCCTTTTAAA | 4215 |
| rs530249887 | snp | G/T | 2.05139e-05 | 0.00320258 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657754 | ATTGAGATAAACTTC[G/T]GTTTTATATTATTTT | 4215 |
| rs530273713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635783 | AGTTTTCTTCATTAC[C/T]AGTTCTTCTGCCAGA | 4215 |
| rs530372291 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692016 | GATTGGTTGAGCAAT[A/C/G]TGAGAGAATATTGCC | 4215 |
| rs530380287 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695670 | CCCCCATCCCCAGTC[C/T]CTGTTCCCCAAGAGG | 4215 |
| rs530416338 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654033 | ATCACACCCAGCTAA[-/T]TTTTTTTGTATTTTT | 4215 |
| rs530550528 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652405 | AACGGTAGAGAAGAG[A/G]AAAAAAGGAAACAAT | 4215 |
| rs530584240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626444 | TTAATTTCACTAAAC[A/G]TTAAAATGTAGTGGT | 4215 |
| rs530599099 | in-del | -/CT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655017 | GAGACAGAGTTGAGA[-/CT]CTGTCTCAAAAAACG | 4215 |
| rs530626316 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652481 | GAAGAAAGGAAGAAT[A/G]TACTCAGACCATTGC | 4215 |
| rs530644185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641026 | AAATCCAAAACATGC[A/C]TTCTGAAACACTTTT | 4215 |
| rs530656909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678156 | CTTTATGGCTTTGGG[G/T]CTTGGGTTTCCCTCT | 4215 |
| rs530704203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640014 | GGTCTTTGAGAGGAG[A/G]ATTGAAATTTGCTCC | 4215 |
| rs530756447 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622360 | AGCGGCTGCCTGGGA[C/T]TGGTGGGGGCCGGCG | 4215 |
| rs530781711 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694018 | TGTCCTGAGCTCAGC[A/G]TGGAGGGGTAGGGGC | 4215 |
| rs530863585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688286 | AGGGCTGTGCAGCCA[A/G]GCTGGAGTTGGGTCA | 4215 |
| rs530900199 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628534 | CCCAGCTAATTTTGT[A/G]GTTTTAGTAGAGACG | 4215 |
| rs530907134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642723 | GTTATGTGTGTGTGT[G/T]TTTTTAACCTCGTTT | 4215 |
| rs530925416 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695486 | TCCCCCAGGGGCTCT[A/G]TCAGCCCCTGTACCC | 4215 |
| rs530925524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687676 | GCCTGGGCGACAGAG[C/T]GAGACTCCATCTTAA | 4215 |
| rs530932217 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627000 | TGGCAACTTTTCTGG[G/T]TTGTTAGCCAAGGGA | 4215 |
| rs530962911 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635734 | TTATTATTATTGTAG[C/T]TTTTGTTAGCCTAGG | 4215 |
| rs530984747 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694835 | AGCTGTGTCCAAAAC[C/T]GCCAGCTCTGTTCTT | 4215 |
| rs531023970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635077 | AGCCACTAGCTACAT[A/G]TGGCTGTTGAGCAAC | 4215 |
| rs531034884 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688021 | ATCTGTAGGGGTGTC[C/T]GTGAAGACAGAAACA | 4215 |
| rs531056437 | in-del | -/T | 0.00159712 | 0.0282137 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627616 | CTGGCTAATTTTGTA[-/T]TTTTTAGTAGAGACA | 4215 |
| rs531096866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642126 | CATATCATGTGGTTC[A/G]TGGAAGCTTGTAAGG | 4215 |
| rs531169028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644864 | ATAATTTTTCTTCAT[C/T]GACTATGACTTCATT | 4215 |
| rs531226258 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641908 | GTCAGAGTGGTAGCA[C/G]GTTCCCTGTGCTGGG | 4215 |
| rs531230584 | snp | C/T | 0.000298602 | 0.0122152 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652565 | TTTTCAGAATTATAG[C/T]GTTCAGCCGGCCTGT | 4215 |
| rs531278794 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660058 | ACCAGCCCAGATATC[A/T]TACCTTAAGTACACT | 4215 |
| rs531352020 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678122 | CCTGTTTTCTCGCTT[C/T]GGCCCCACCATAAAG | 4215 |
| rs531410996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660667 | GTGTGATCTTGGCTC[A/G]CCGCAACCTCTGGCT | 4215 |
| rs531470444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673629 | ACTAAAGGACTTGTC[A/G]GCGGGGTGCAGTGGC | 4215 |
| rs531474307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659883 | ATGGAAAAATAAACT[A/G]GAGGTATATAAATTA | 4215 |
| rs531536209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665879 | GCAGGAAACCTTTTT[C/T]CTGGAGGACAGGATA | 4215 |
| rs531591243 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675467 | TCTGCTATGAGAAGG[A/G]CTAGAATCTGAGAGC | 4215 |
| rs531603473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665299 | GCCTCCTGAGTAGCT[C/G]GGACTACAGGTGCCT | 4215 |
| rs531612057 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644626 | CTCTTTGGGGTCTTT[A/C]ATAATTTTTACAGTG | 4215 |
| rs531720116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623711 | TTTTAAACGTTCTTT[A/T]CTTCTCCTGCCCAGA | 4215 |
| rs531736726 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650823 | CAGCCTCCCAAGTAG[C/T]TTAGACTATAAGCAT | 4215 |
| rs531742546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675105 | AGATCAGAAACTTTG[A/G]TGGTGGTAGCAGCTC | 4215 |
| rs531762538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631191 | ACTCTGGAGGCTGAG[C/G]TGGAGGATTGTTTGA | 4215 |
| rs531903995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622774 | CATGGGTAAGTGTCG[C/T]CACCGCCCCGGCCTG | 4215 |
| rs531929636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682361 | TGATCATTTATGATG[A/G]TAGACAGTTGTATTA | 4215 |
| rs531968088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637568 | ATGTGAAGTTGCAGT[A/G]GTTATGTCACTTCTT | 4215 |
| rs531993680 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691183 | TACTATGGCTGTCTG[A/C]GGGACCGCGCTGAGA | 4215 |
| rs532031600 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631641 | CAACATGGAATTGGA[C/G]TGGTTTGTGTTCTGG | 4215 |
| rs532034012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659818 | CAGGCATGAGCCACT[A/G]TGCCCGGCCGTACCA | 4215 |
| rs532145784 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672208 | GAATTGTTTGAACCC[A/G]GGAGGCGGAGGTTGC | 4215 |
| rs532152373 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620551 | TACTAATTTTCTTTC[C/T]CCTTTATCCCCGCTT | 4215 |
| rs532155204 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649281 | GTCTCTACTAAAAAT[A/G]TAAAAATTAGCTGGG | 4215 |
| rs532248833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628468 | CAGCTTGAAGCAGTT[C/T]TCCTGCCTCAGCCTC | 4215 |
| rs532278692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679659 | TTTAAAATATTTTTT[A/G]TAGAGATGGGGTCTC | 4215 |
| rs532310828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635611 | GTAAGAGGTAGTGCG[A/G]GGAAGATGTTGGGGA | 4215 |
| rs532320211 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679016 | CCTGGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 4215 |
| rs532336978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688218 | CCTGGGCAAAGGATT[A/C]TCTTGGAGCTCTTTG | 4215 |
| rs532340228 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633066 | AACCCTGTCCCTACT[-/A]AAAAACACAAAATTA | 4215 |
| rs532359502 | snp | C/T | 1.66095e-05 | 0.00288175 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652562 | TTCTTTTCAGAATTA[C/T]AGCGTTCAGCCGGCC | 4215 |
| rs532438976 | snp | A/G | 0.030665 | 0.119967 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622528 | AGGCCGGGCTGGGCC[A/G]AGCCCAGGAGCGCCC | 4215 |
| rs532442002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627998 | GCAACCTCTGCCTCC[C/G]AGGTTCAAGCTATTC | 4215 |
| rs532443432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674433 | TGCAGTGGTGCCATC[A/G]TGGCTCACTGCAGCC | 4215 |
| rs532473050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679028 | AGCAAGACTCCGTCT[C/T]AAAAAAAAGAGTCAG | 4215 |
| rs532496759 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645704 | AAATGTATCCTGGTC[A/G]GGAGGTGATAGAGTG | 4215 |
| rs532505334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629941 | TGATTTCTTCAGTCA[C/T]ACTTGTGGATCTGAC | 4215 |
| rs532513223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623571 | GTATTTACAATTTCT[A/G]CTGTGAAGATGTAAT | 4215 |
| rs532535654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636990 | TGGGCTACGGTATCC[A/G]GAAGCTGCAGATTCA | 4215 |
| rs532563624 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687662 | GCCACTGCACTCCAG[C/T]CTGGGCGACAGAGCG | 4215 |
| rs532593723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636677 | TGTCTCCCATGTGCC[A/G]AGTGGAGCCCCCAGC | 4215 |
| rs532596077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644717 | TTGGGAAAAGGGAGT[C/T]CTTTAGGCATCTACC | 4215 |
| rs532656171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643537 | ATAATAATAATAGGG[A/G]AAACTGTACAAAGGG | 4215 |
| rs532716172 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659790 | CCCGCCTTGGCCTCC[C/T]AAAGTACTGGGACAG | 4215 |
| rs532755630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631824 | ATGGGAAGTAGTAGG[C/G]CTATAAACTTGTAAA | 4215 |
| rs532801058 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693047 | CAATGAAAGCAAGAG[G/T]TTGGAGTAATACAAG | 4215 |
| rs532872760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696421 | TCAAGCAGAAGAGAA[C/T]TTGACTCCAAGTAGA | 4215 |
| rs532881627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691423 | GGTTGCAGTGGGAGT[A/T]TGAGATGACAGCTGT | 4215 |
| rs532984860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638576 | TCAACCCGACAGCCC[A/G]CACTGTCTCTCTCCT | 4215 |
| rs533035539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646609 | ACATAGAAAGAGGGA[A/G]TTTTTCGGTCTGTGT | 4215 |
| rs533110089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654132 | CCTCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 4215 |
| rs533110456 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645835 | TACCCTAAGAGCTTT[G/T]TTGTCCCTGATGTTA | 4215 |
| rs533244188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655220 | GAGAAAAAGCCTCCT[A/G]TAAAACCATCAGATC | 4215 |
| rs533308429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660814 | TTGGTCAGGCTGGTC[C/T]TGAACTCCCGACCTC | 4215 |
| rs533357404 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638246 | TTTTTTCCTTTCATT[C/T]ACTTACTCTCTTTGG | 4215 |
| rs533388703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655958 | TTTTTGGCGAGGCGC[A/G]ATGGTTCATGCCTGT | 4215 |
| rs533458900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624816 | AAGTAGATGACCTTG[A/G]TACACTGTTAGAGCT | 4215 |
| rs533483498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675743 | GGTGGCACAGGTGGC[A/G]CAGTGAGGCTAGAGC | 4215 |
| rs533503956 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662745 | TCACCGCAGCCTCCA[C/T]CTCCCGGGTTCAAGC | 4215 |
| rs533582842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629423 | AGCCTCTGCGCCCAG[C/T]CTGTTATTTGTTTTT | 4215 |
| rs533633460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668678 | CTGGACCCTTTCTCC[A/G]TGTTACCGGGAGCTA | 4215 |
| rs533641052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636812 | AGTGGCTGAGGTGGT[A/G]TGTGGAGAAGAAGGC | 4215 |
| rs533668510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632457 | TGATCACGCCACTGC[A/C]CTCCAGCCTGAGTGA | 4215 |
| rs533708426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684217 | CTAACCATAAAGAAC[A/G]TCATTTTTTACAAGA | 4215 |
| rs533736999 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665014 | AGGTGTCAAAATCTC[C/T]ACAGGCAGCTGGGCA | 4215 |
| rs533748090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630266 | AGCCAATCTTCCTAG[C/T]TTAGATGTTATGCTC | 4215 |
| rs533770034 | snp | A/G | 1.74821e-05 | 0.00295647 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63681815 | TGGCTATGTTCCTGA[A/G]CGGCAGCAGCACATT | 4215 |
| rs533770115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674065 | AGCTTAGGCAACAGA[A/G]TGAGACTCTGTCTCA | 4215 |
| rs533887287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659218 | AATTTGTAAGGATAC[A/G]TGTTTCTCTTGAGTC | 4215 |
| rs533944423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636041 | CTACAAGGCAGAGTC[A/G]AGACTGGCACAGCTT | 4215 |
| rs533949737 | snp | C/T | 1.70758e-05 | 0.00292192 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646007 | TTCCAGAGAATTCTC[C/T]AACCTGTCTATCATT | 4215 |
| rs533994999 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652213 | CAGCCCCAGTGTGTA[G/T]TGTTCCCCCTCCATG | 4215 |
| rs534006373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645196 | AACATGATAGACCTC[A/G]GGAGGCCGAGGCAAG | 4215 |
| rs534039546 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696050 | CACTTTCTCATCATT[C/G]CATGGGGTGTGTCTG | 4215 |
| rs534045656 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667609 | ACCCCTGTGGATGCC[A/G]AGGTCTGTGGATGCT | 4215 |
| rs534059351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651467 | TGACAGAACGAGACT[C/T]TGTTTTGAAACAAAC | 4215 |
| rs534199832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667113 | ATCTGCCCACATTTT[A/T]AAAAAGCAACAAGTA | 4215 |
| rs534224761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623204 | TTCCTGCCTGTGTCA[G/T]TTCCTTCCCTTTGCT | 4215 |
| rs534333552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654803 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 4215 |
| rs534348955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661697 | TTGTAAGTTAAAAAT[A/C]TCAAGGATAATTTAA | 4215 |
| rs534446988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668989 | CATCAAGTAGAGAGA[G/T]ATATCTCAGGCATAG | 4215 |
| rs534508281 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675930 | ATGGTCCAGTATCCT[A/C/G]TCCTGTTTAGCTCCC | 4215 |
| rs534542993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666467 | AGCAAGACTCTGTAT[C/T]AATCAATCAGTCAAT | 4215 |
| rs534565490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675515 | GTCAGAGTACAAAGC[A/G]AAAGAACCTACCATA | 4215 |
| rs534619821 | snp | C/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677802 | AGCCCAAGGAGTTTG[C/G]GGCTACAGTGAGCTA | 4215 |
| rs534654854 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633229 | GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 4215 |
| rs534677371 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627460 | CTTTTTTTTTTTTTT[G/T]GGGGTGGAGTTTTGC | 4215 |
| rs534705593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678343 | AACTTTAGTTTCTGT[G/T]AGGACTTAGAAAATA | 4215 |
| rs534712745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625817 | TGGCTTACACCTATA[A/G]TCCCAGCACTTTGGG | 4215 |
| rs534738177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634229 | AGAAGTGAGTCCCCT[C/T]CCCCTTGCTTGAGCC | 4215 |
| rs534768390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686947 | TTGAATGGCTTCAGA[C/T]AAGTCTTTTAACCTC | 4215 |
| rs534777669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625007 | TAGTTGCTGTAGTTC[G/T]AAATAAACTCAAAGG | 4215 |
| rs534856779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632921 | TTTTGACCCCTTCCT[C/T]TCACAGTCTGTTAAA | 4215 |
| rs534876507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683685 | TCTGCTTAACAGGAA[C/T]GAACACTGCATAGTA | 4215 |
| rs534884769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684997 | TATTACCTCTGCATT[A/G]GACCAGGAACTGGGA | 4215 |
| rs534909522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638805 | TAACCCCAACACTTT[A/G]GGAGGCCGAGGCAGG | 4215 |
| rs534947043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693102 | CAGGTGGCCTCTAGA[A/G]CCCAGGAAAGGCAAG | 4215 |
| rs535006609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670977 | TGATGTTACATATTC[A/G]TATTTGTATTTTGAA | 4215 |
| rs535106309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633622 | ATGCTTCTTTAGGAA[A/G]ACATTGCCTATTTTC | 4215 |
| rs535173162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667962 | TGCATTATTACTTGT[C/T]AACCCAGGATTCCTG | 4215 |
| rs535230755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675455 | CCTGATTAGGGTTCT[A/G]CTATGAGAAGGGCTA | 4215 |
| rs535233200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660893 | GAGCCACTGCACCCC[A/G]CCTTGGATTCTTCTG | 4215 |
| rs535247009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648675 | CAAAAATTAGCCGGG[C/T]GTGGTGGCCGGCGTC | 4215 |
| rs535255661 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624588 | TCTAGAGCCCCAAAG[-/A]AAAAAAGGGCCAGGA | 4215 |
| rs535292514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673167 | ATATTTGAAATTCTT[A/C]TTTATTTTGGATTGA | 4215 |
| rs535313207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648012 | ACTGTCCTCCCTTTT[A/G]GCCCCAGGAGGGCTG | 4215 |
| rs535326507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682004 | TGAGGGACATGAACC[A/C]CATTTGAAAGCTCTT | 4215 |
| rs535326579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691502 | GTAAATGCAGCCTTC[A/G]TCTGGAGCAGAGAGG | 4215 |
| rs535383549 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666210 | CCTCTGTCTGGCACA[A/G]TGGTACTTATGATAG | 4215 |
| rs535416696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625992 | GTGGGAAGATCATCT[A/G]AGCCTGGGAGGTTGA | 4215 |
| rs535423169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668781 | GAAAATGGGCAACAC[A/G]GCCTCTTAGCATACC | 4215 |
| rs535427198 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669472 | ATTTATTATGTTGTC[-/T]TTTTTTTTTTTTTCT | 4215 |
| rs535428782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645136 | AAATATTATTAAGCA[C/T]AAATATTATATGCCA | 4215 |
| rs535439031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633410 | CAGAAGGTTTTTAGC[C/T]ACCTTACAGTATATA | 4215 |
| rs535464063 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657440 | GAAATGTCCAGAAAA[C/G]GCAAATCAATAGAGA | 4215 |
| rs535480869 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624912 | TATACACAGATACAT[G/T]CACACACAGTCTCTC | 4215 |
| rs535543834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624060 | TTTGCTGGGCTTACT[A/G]TTTCCTTCTCATGCT | 4215 |
| rs535666142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630611 | GGATTACAGGCATGA[A/G]CCACCCTGTCCAGCC | 4215 |
| rs535677363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647083 | CTCTACAGTTGGTAC[C/T]TTTCAGCCTACTTTG | 4215 |
| rs535724632 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645969 | CTGCCCAAGGCTTAC[C/T]TGGCAATGGCAGGAG | 4215 |
| rs535844434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677015 | AATCCATCTTACGCC[A/T]ACCCCATATATCTGC | 4215 |
| rs535904585 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629160 | ATGGAGTCTCGCCCT[C/G]TCGCCATGCTGGAGT | 4215 |
| rs535922544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648777 | CCGAGTTCGAGCCAC[C/T]GCACTCCAGCCTGGG | 4215 |
| rs535924561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656958 | GCGACAGGAGAGAGA[A/G]GTGCCAAGCAAAGGG | 4215 |
| rs535925665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639536 | AACAAAGAAGGAACA[C/T]GGTGAAAAAGGTGAT | 4215 |
| rs535991250 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661569 | AATATCAAGCTGAAC[C/T]TTCTTTTGTAACTTG | 4215 |
| rs536007253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663970 | GCTTTAGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 4215 |
| rs536061781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655493 | GTCACTGTGAGTTTT[A/G]TTTTTGTTTTTGGTT | 4215 |
| rs536136105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626486 | ATTCTTATGAGGAAT[A/C]AATGGCCTACTTTAT | 4215 |
| rs536179440 | in-del | -/TTTTTTTTTTTTTT | 0.149999 | 0.229128 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659526 | AAATCTGTCATGGAC[-/TTTTTTTTTTTTTT]TTTTTTTTTTGGAGA | 4215 |
| rs536185222 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63670078 | ATGGTACTCCAGCCT[C/G]GGCAACAGATCAAGA | 4215 |
| rs536185515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662218 | TGAGACCAGCCTGAG[C/G]AACATGGCGAAACCC | 4215 |
| rs536200419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641417 | CCGGCTAATTTTTGT[A/G]TGTTTAGTAGAGACG | 4215 |
| rs536271766 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620842 | AAACCCCGTCTCTAC[C/T]AAAAATTCAAAAATT | 4215 |
| rs536351100 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637433 | GTCATATAACCTTTC[C/T]GAAGTGAGTTTTTCC | 4215 |
| rs536442079 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679255 | CTCCCCGCCATTCTT[C/T]TTTTCCATTAAGTAT | 4215 |
| rs536453483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663448 | CGGAGGTTGCAGTGA[A/G]CCGAGATTGTGCCAT | 4215 |
| rs536527857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642276 | TTCATGTAGAGCAGT[C/G]CTTAGGTTATGGCTC | 4215 |
| rs536680279 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620818 | GAGACCAGCCTGGAC[A/G]ACATGGCGAAACCCC | 4215 |
| rs536711380 | in-del | -/A | 0.0023933 | 0.0345097 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620675 | AAAAGAAAACAGGAC[-/A]AAGGGGGCTGATTAA | 4215 |
| rs536712965 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663395 | CAATCCCAGATACTC[A/C/G]GGAGGCTGAGGCAGG | 4215 |
| rs536722173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664991 | TGTCCAGAGGTTCTG[C/T]TGATCTGAGGTGTCA | 4215 |
| rs536839851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669948 | TCTCTACAAAAAATA[C/T]AAAAATTAGCCAAGT | 4215 |
| rs536845456 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651434 | GCCGTTATCATTGCC[A/G]CTGCACTCCAGCCTA | 4215 |
| rs536924664 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643790 | TGTGGGAAGCTGGAG[A/C]CCACACATCAGAGCA | 4215 |
| rs536943794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634427 | AGGAGGGGCGGAATG[G/T]TCACTGATGGTTCCT | 4215 |
| rs536945230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625162 | ATTTTCCTGAGCTGT[G/T]CTAAGCCCAAGACTG | 4215 |
| rs536965236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676000 | CCCAATTTCTGAAAT[A/G]AAGATTAAAAACAAA | 4215 |
| rs536970710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687164 | TGAGGTCAGGAGTTT[A/G]AGACCAGCCTGACCA | 4215 |
| rs537013723 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671444 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCACGT | 4215 |
| rs537041232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685143 | AAATTATAAATTATG[A/G]AGTGTAAACAGAAGC | 4215 |
| rs537105407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679239 | CACACACAGAGCAAG[C/G]CTCCCCGCCATTCTT | 4215 |
| rs537224560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687140 | GGAAGCTGAGGCACG[C/T]GGATCACCTGAGGTC | 4215 |
| rs537285524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625920 | CTACTAAAAACACAC[A/G]AACTTAGCTGGGCGT | 4215 |
| rs537286490 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686158 | ATTGATCTTGCCACT[A/C]CCTCGCCTCTGCCTC | 4215 |
| rs537288245 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694262 | GGAAAGGCCAGCACT[C/T]GCTAGCAGTGGCAGG | 4215 |
| rs537315845 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686041 | AATGCCTAGTGTACC[A/G]TGCCACCTGCTTGGT | 4215 |
| rs537329428 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649391 | GCAGTGAGCCGAGAT[C/G/T]GTGCCACTTCAGCCT | 4215 |
| rs537365318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684667 | ATTAATTAAAAAAAT[A/G]TTTAAACAGAAACAA | 4215 |
| rs537386258 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624396 | GTAGACCATCCACTT[C/T]CTACTTTGTTGACTG | 4215 |
| rs537410049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636772 | AATGAGGAGGAAGAC[A/G]AGGAGGCAGCCCGGC | 4215 |
| rs537508570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671396 | AAGTAGCTGGGACTA[C/T]AGGCATGCGCCACCA | 4215 |
| rs537604975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634339 | GACTGGACTATTAGC[A/G]TGAATATCAGTTAGT | 4215 |
| rs537625014 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656365 | CCCACCAGTTTGGTA[A/G]GCTGAGGTGGGCAGA | 4215 |
| rs537650340 | in-del | -/A | 0.153 | 0.230415 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681113 | ACCCTGTCTCAATTT[-/A]AAAAAAAAAAAAAAA | 4215 |
| rs537725701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640390 | TACAGTGGGAAAAAA[A/C]CTCAAGAGTGTGTGA | 4215 |
| rs537781107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678012 | CAAGGAGAAGTTATG[C/T]CTTGTGCCACTGTGT | 4215 |
| rs537819722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680203 | ACCAGCCAGCAAGGA[A/G]AGTAACCTGCATTGT | 4215 |
| rs537851183 | in-del | -/TTC | 0.0180209 | 0.0931971 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660566 | TTTCTTCTCTTTGGA[-/TTC]TTCTTCTTCTTCTTC | 4215 |
| rs537870676 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642977 | CGCCCAGACTGATCT[C/G]AAACTCCTGGGCTCA | 4215 |
| rs537915741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660916 | TTCTTCTGATCCCTA[C/T]ATGGCAGCTTCTAAT | 4215 |
| rs537979040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660349 | ACTGGGACTACAGGC[G/T]TGTGCCCCCATGCTT | 4215 |
| rs537990954 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642515 | ATACAAAAATCATTC[A/G]GGCATGGTGGTGCAT | 4215 |
| rs538020674 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672985 | CCTTGGTTAGTAAGC[C/T]TTAGCAATTCAGCCT | 4215 |
| rs538029873 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695325 | TATCTCAGATCATAT[A/T]TGATGGTTTTTATAT | 4215 |
| rs538042855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659127 | TCCACCCACTTTAGC[C/T]TTGCAAAGTGCTGGG | 4215 |
| rs538048203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666305 | CAGGGAGTGATTATT[A/G]TTGGGAAAAAGAAGC | 4215 |
| rs538088453 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621924 | GCGGGGAACTGCGCC[A/T]GCCCGCGCGCCCGCC | 4215 |
| rs538104328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658193 | TTGTGCTCTAAATTT[A/T]TGTTTTTTCAATTAG | 4215 |
| rs538148576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629340 | ATGTTGGCCAGGCTG[A/G]TTTCGAACTCCTGAC | 4215 |
| rs538184024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638951 | GAATCGCTTGTACTT[A/G]GGAGGCGGAGGTTGT | 4215 |
| rs538199936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642919 | TGTGCCACCACAACC[A/C]GCTAATTTTTGTATT | 4215 |
| rs538405229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658017 | AGCCACTGCCAAATT[A/G]AGAGCATAAGCACAG | 4215 |
| rs538478693 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675698 | TCTCTCTGAACAGTG[A/G]AACTGCTACTGTGCT | 4215 |
| rs538525398 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621061 | CAAGGTAATTCTTAA[A/G]GGATTTGACACTCAA | 4215 |
| rs538547827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673043 | GCCATCATCGTTTAC[A/G]TACATGTGAATATTT | 4215 |
| rs538555074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680869 | GTTAAGTAAAGCAAA[C/T]GCTTACCTCTCAGGA | 4215 |
| rs538582635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663496 | GATGAGCGAAACTCC[A/G]TCTCAAAAAAAAAAA | 4215 |
| rs538608834 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687790 | GTCAAGAGATCGAGA[A/C]CATCTTGGCCAGTGG | 4215 |
| rs538616546 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695740 | AGGTTCAGGGTCTTA[C/T]AGAGCTCCACCCCCT | 4215 |
| rs538681305 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695186 | CATGCCTACATCCCC[A/G]TGGGCACAGAACAAG | 4215 |
| rs538743267 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694494 | AATGCAGTTGTCTCT[C/G]TTTTACAAGTTGGAG | 4215 |
| rs538774883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673847 | CCTGGGAAGCAGAGG[A/T]TGCATTGAGCCAAGA | 4215 |
| rs538821560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642376 | AATATAATGTTGTCC[C/T]AGGGCTGGGGCAGTG | 4215 |
| rs538824138 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620903 | CCCAGCTACTTGAGA[A/G]GCTGAAGCAGGAGAA | 4215 |
| rs538839178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656989 | GGAAAAGCTCCGTGA[C/G]AATGGAGGAGGTAGT | 4215 |
| rs538860359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639841 | TTACAAAATATAATG[C/G]CAGGCTTGTGTGTTG | 4215 |
| rs538887852 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628736 | AGTTTGAACACCTTG[A/C]AATATCTTTTAAAAC | 4215 |
| rs538896079 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672085 | ATTAGGAGTTTGAAA[A/C]CAACCTGACCAACAT | 4215 |
| rs538924612 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684172 | CAAAATGCTAGCACA[A/G]TGTAACGTCCTTCAC | 4215 |
| rs538935665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635842 | GAAAGATCAAAACCT[A/G]ATTTAAATGGTGAAG | 4215 |
| rs539023893 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629613 | AGGAAGAAATGCCTA[A/G]AAGAGCCACTTGATT | 4215 |
| rs539087385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659626 | CAACCTCCACCTCCC[A/G]GGTTCAAGCAATTCT | 4215 |
| rs539128594 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621816 | CACCCTCTGGAACCA[C/T]CCAGATCGCTGGGGC | 4215 |
| rs539258221 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636422 | AGCGTGGTTAGAGCT[C/G]ACTGAATATTCTTAG | 4215 |
| rs539309242 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661985 | GCAGGTGCCTGTAGT[C/T]CCAGCTACTCGGGAG | 4215 |
| rs539332830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679467 | TACAGGCTGAGTGCT[C/T]CTGGCTCCACATGAG | 4215 |
| rs539400874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652331 | GATGAATGGTTGGGA[C/T]TGAGCAATAGTTGTG | 4215 |
| rs539409381 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632130 | CTGCCCTGTTTGAGC[A/G]TGTCCCTTCCCTGCA | 4215 |
| rs539427145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683925 | ACTTTGGGAGGCCAA[C/G]GCAGGAGGATTGCTT | 4215 |
| rs539430849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667165 | AAATATTTATTAACT[A/G]TTACTCTGTGTAGAG | 4215 |
| rs539472711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638885 | ACAAAAATTAGCTGG[A/G]CATGATGATAGGTGC | 4215 |
| rs539474104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682708 | TGCCATGGGGCCCTC[C/T]CACAACATGGCAGCT | 4215 |
| rs539594040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637133 | TTAGAGTGTGTGTGC[A/G]TGCATGCGCACGTGT | 4215 |
| rs539596549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646284 | ATTGGAAGCCATTTC[A/C]ACTGCTGATGTTTTA | 4215 |
| rs539657900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645094 | CATATTTATACTTCT[A/G]TTCTTCAATTCATTC | 4215 |
| rs539847085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665632 | TGCAAGACTATGACC[C/T]TCCCTTGCCCTTCAC | 4215 |
| rs539868409 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621282 | ATGGTGCCTTTAATT[G/T]TGAAACATCATGCAA | 4215 |
| rs539884266 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673348 | ACCTTGAATTCCAGG[-/T]TTTTTTTCAGGCCAT | 4215 |
| rs539889622 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679319 | GAGTCTCTCTGGCTC[A/G]GGGAGTTTGTTGAGC | 4215 |
| rs539908272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646947 | CCCTGCCACCCTCAG[C/G]TTTCCTTTGCTTTGA | 4215 |
| rs539994436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628438 | CCATCTTGGCTCACC[A/G]CAACCTCCGCCTCCC | 4215 |
| rs540035547 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628503 | GTAGATGGGATTACA[A/G]GCATGTGCCACCACG | 4215 |
| rs540038613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662174 | ACTTTGGGAGGCTGA[A/G]GCAGGCAGATTACTT | 4215 |
| rs540070733 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626337 | ACATGTAAACAATTA[A/C]GTGCAAAAGTGTGTA | 4215 |
| rs540135346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642606 | GAGGCTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 4215 |
| rs540162523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667822 | AATCTGTGGTTGGTT[A/G]AATCCACAGATGCAG | 4215 |
| rs540163940 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695372 | GTTACAGGTGACGGA[C/T]GCCTCAAGAGAGAGA | 4215 |
| rs540308795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681553 | GTTTTTTTGGTCGGA[A/T]ATGCCGTAGTGCCTG | 4215 |
| rs540315990 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628869 | AGTCTTTTTCCATTG[A/G]CCTTTTCTCATTGAT | 4215 |
| rs540343817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636939 | CTTCATCCAGCTGGA[C/T]GGGCTGGTCTAGGGG | 4215 |
| rs540353255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680349 | CAGGATAAATTTGTT[C/T]CCTTCAGAACAGGAA | 4215 |
| rs540368144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644705 | TCCCTTAATACCTTG[C/G]GAAAAGGGAGTCCTT | 4215 |
| rs540374631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690119 | GGCACTGGGCTTGCT[C/T]CAGATTGTGGTGGAG | 4215 |
| rs540414457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679614 | CAGTCTTCCAAGTAG[C/T]TGGGTCCACAAGTGT | 4215 |
| rs540429457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652477 | TTGAGAAGAAAGGAA[G/T]AATATACTCAGACCA | 4215 |
| rs540429585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643493 | TCCAGCTTGGGTGGC[A/G]GGAGTAAGACCCTGT | 4215 |
| rs540450675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662264 | AAAAAAAAAAAAAAC[C/G]AAAATTAGCCAGGTG | 4215 |
| rs540451529 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642321 | TTAGTTCCTTCATTT[C/G]CATAAAGGCACTGAG | 4215 |
| rs540501790 | snp | C/T | 0.000727477 | 0.0190581 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634736 | AGCAGCAGCTCAGCC[C/T]TTCTGAACAGCCCCA | 4215 |
| rs540530432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687521 | CGTCTCAAAAAGAAA[A/G]AAAAAAAAAGCAAAA | 4215 |
| rs540571947 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630985 | CGTCTAGGAAGAGGG[A/G]AGAGGCAAATAAGGT | 4215 |
| rs540574566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650844 | CTATAAGCATGTACT[A/G]TCACACCTGGCTAAT | 4215 |
| rs540575776 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666149 | GCCCAGTGGAAAGAG[C/T]GGGTGGGTGCTGGGA | 4215 |
| rs540599320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682071 | TTTTAAGGGCCAAAT[A/G]ACAATTTCTGCCAAA | 4215 |
| rs540635966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637380 | GAAGTAAATCCAAGC[C/T]TTCTGATTCCTAGTC | 4215 |
| rs540664406 | snp | A/C | 0.000303567 | 0.0123163 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691008 | TTCCCAAGGCAGATC[A/C]CTGTGAGGCCACTAA | 4215 |
| rs540697625 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652240 | CATGTGTCTGTGTGT[G/T]CTCATCGTTGGAACA | 4215 |
| rs540704596 | in-del | -/TTC | 0.306428 | 0.243548 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660568 | CTTCTCTTTGGATTC[-/TTC]TTCTTCTTCTTCTTC | 4215 |
| rs540753861 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625748 | ATTACTAGATTTCTG[A/G]TATTTTTAAAAATGA | 4215 |
| rs540868255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661382 | CTCTCTCTAGCCTTG[A/G]TCTCTACCATCATTT | 4215 |
| rs540888217 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668742 | GAGGAGTGAGATTTC[C/T]GTGAAGTAGTTCCTG | 4215 |
| rs540950497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674825 | AGGAAGAGAGGAGCC[C/T]TCTCTGCCTCTGAGA | 4215 |
| rs541010988 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654008 | AGTAGCTGGGACTAC[A/T]GGCACACACCATCAC | 4215 |
| rs541088209 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621679 | GGGCAAGAGCAGCGT[C/T]GGGACCGGAGGACCA | 4215 |
| rs541094873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653969 | CCTCCTGCGCTCAAG[C/G]GATTCCCCCACCTCA | 4215 |
| rs541117666 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662626 | TGTAGTCTAGTGCCT[G/T]TCAGTCACCATCCAG | 4215 |
| rs541140201 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656945 | CATCCTTCATATGGC[A/G]ACAGGAGAGAGAAGT | 4215 |
| rs541191059 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647323 | TAGCAGAGAAGTTAA[A/G]TTGTCACTTCACTGT | 4215 |
| rs541253213 | snp | A/T | 0.00071254 | 0.0188617 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634727 | AAACACAACAGCAGC[A/T]GCTCAGCCCTTCTGA | 4215 |
| rs541320536 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682481 | TCCAGGCATGACTCA[A/G]ATGGGTCCTCTGCTG | 4215 |
| rs541398651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662994 | AAGAGGGTTCTTAGA[A/G]TTATTGTAGTCCTTG | 4215 |
| rs541403321 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694731 | TGATCCCAGAGAGCC[C/T]GAGGAGGTGTCTCAG | 4215 |
| rs541479060 | snp | C/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621902 | CACCCCAGCCCTAAA[C/G]TAGCCGGCGGGGAAC | 4215 |
| rs541489795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63670115 | CTCAAAAAAAAAAAA[A/T]GTAATTACCAAAGTA | 4215 |
| rs541552930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677093 | GAGATGGGGTTATGC[A/G]GATATGTACCTGTGC | 4215 |
| rs541553183 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669412 | TTTTGGTAGGCAGTG[A/G]AAGCCACTGAAAATG | 4215 |
| rs541565723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625329 | CTATAAAAAATTGGG[A/G]TTGACTGGTTGTTTT | 4215 |
| rs541599476 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651193 | ATACATTCATTCAAA[C/G]TTTTTATTGGCCAAG | 4215 |
| rs541616374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676333 | CCAGGGGAGAGTTCA[A/G]TGCAGCTGATGAAGG | 4215 |
| rs541619167 | snp | C/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690063 | TGACTTCAGCCAATC[C/G]TCTGCTTCTTAGGAC | 4215 |
| rs541625948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632387 | TTCCCAGCTACTCAG[A/G]AGGCTGATGTGGGAA | 4215 |
| rs541653863 | in-del | -/GGAGGAAACAAGTGGTGT | 0.00279162 | 0.0372561 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686080 | TCTTCTTACACTTTG[-/GGAGGAAACAAGTGGTGT]CCTTTACATACCAAA | 4215 |
| rs541655557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666633 | AGGGTATTTACAGCT[C/G]TCTTTTCTGTTTTGC | 4215 |
| rs541681095 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622284 | GGAGGGGGACGGCGG[A/G]GGCTGCCGACTTCCT | 4215 |
| rs541715516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654643 | CTGCCCAGATTTTCT[A/G]TAATGGTTGCACAAT | 4215 |
| rs541715623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674328 | CCAGCACTTTGGGAG[G/T]CCAAGGTGGGTGGAT | 4215 |
| rs541723463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639016 | ACAGAGCAAGACTCC[A/C]TCTCAGAAAAAAAAG | 4215 |
| rs541742550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681346 | CCCTCAAAATACTGC[G/T]TGGACCCAAAACTAA | 4215 |
| rs541777442 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688495 | GCTGTGGAAGTGTGC[A/G]GGAGTCTGTTTTTTC | 4215 |
| rs541784517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638509 | GTCATTTCTGCTTTA[A/G]TGTTATTGTCAGTTA | 4215 |
| rs541890196 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686232 | GACTGTGGTCAGAGG[C/T]TATGGAAAAGGTTTG | 4215 |
| rs541904175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632272 | CGAGGCAGGAGGATC[A/G]CTGGAGTCCAGGAGT | 4215 |
| rs541917392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661327 | GCTGAGATTACAGGT[A/G]TGAGCCACCGGATCT | 4215 |
| rs541919751 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631174 | CACCTGTAGTCCCAG[A/C]TACTCTGGAGGCTGA | 4215 |
| rs541920040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668445 | GCAAGGAGAGCCTAG[C/T]CACAGCGTCTCTGGC | 4215 |
| rs542002914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652402 | GGTAACGGTAGAGAA[A/G]AGGAAAAAAGGAAAC | 4215 |
| rs542202207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677272 | AGTCTTTTCTCCGTG[C/T]ACCTCACTTACCTCC | 4215 |
| rs542202558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645508 | ATTGCATGTCTATTA[C/T]GTGTCAGGTATTTTA | 4215 |
| rs542260882 | snp | A/G | 0.0001812 | 0.00951667 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685519 | ACTTGCCTTACAGAT[A/G]CTGGATCCCCTGAGC | 4215 |
| rs542299432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676145 | CAATAGCCGCTGGCA[C/T]ATAGCCCATCAGATA | 4215 |
| rs542301025 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665201 | CCCAGCTACTCGGGA[C/G]GCCGACCAGGCTGGA | 4215 |
| rs542302618 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693887 | TGTGGACCATGGAGT[A/G]GCAGCCCAGCCAGCG | 4215 |
| rs542366838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675693 | GGGCCTCTCTCTGAA[C/G]AGTGGAACTGCTACT | 4215 |
| rs542366852 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684054 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGTGG | 4215 |
| rs542418281 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647443 | GAGCCCAATTACGCA[C/G]TTAGGCTCTCCTGAA | 4215 |
| rs542432112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682861 | CACAGGTTCTACTTG[C/T]ACTAAAGGGAAAGGC | 4215 |
| rs542485585 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655013 | ATTTGAGACAGAGTT[G/T]AGACTCTGTCTCAAA | 4215 |
| rs542511813 | in-del | -/GA | | | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696085 | GGCCAACTCTGCATG[-/GA]GAGGCCAGGGCTGGG | 4215 |
| rs542789887 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664119 | GGGCGTGGTAGCGGG[C/T]GCCTGTAGTCCCAGC | 4215 |
| rs542882004 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648381 | TGTTGCTGAGGCCTT[A/G]AAGAAGGAGGGGTAT | 4215 |
| rs542940596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662429 | CGAATAATAGTAATA[A/G]TAACAACACCTAGCA | 4215 |
| rs542978870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693154 | GCCTCTGACAGGAAC[C/T]AGCCCTGCCGCCACC | 4215 |
| rs542979180 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694686 | GGGAGATGGACGACA[C/T]GGTCGGGGCATCTGG | 4215 |
| rs543045929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649925 | CTTGTGGCTTATTGC[C/T]TCTTCCTCTGGTTAC | 4215 |
| rs543059823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648119 | TGTTAGACCTCTCTT[G/T]GAAGCACTGGCCTAA | 4215 |
| rs543062447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692769 | CAGTTTGCACTTGCT[C/T]GACATAACCTTGTGT | 4215 |
| rs543205570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662382 | ATTGCAACACTGCAC[C/T]CCAGCCTGGGTGACA | 4215 |
| rs543243728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654158 | ACAGGCATGAGCCAC[C/T]GCACTTGGCCTCCAG | 4215 |
| rs543317602 | snp | A/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620961 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 4215 |
| rs543323610 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622584 | TGCCACAGCGCCCGG[C/T]CGCGGGCGGAGCCGG | 4215 |
| rs543450813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639106 | GTGAGGACTACATGA[A/G]AAAAAGAAAGTATGA | 4215 |
| rs543478390 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682038 | TAAACCAGGCCTGCC[C/G]AAATATGGATTGTCC | 4215 |
| rs543502966 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651713 | TTATATTTGTAGAAA[C/T]TGTTCTTTGAACTGA | 4215 |
| rs543568176 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671054 | AATGCATGCAAGGGA[A/G]CTGCATTAGGCTAAT | 4215 |
| rs543614809 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626841 | ATTGTCAAGATGAAG[A/T]AATAACATCATTAGT | 4215 |
| rs543634721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677878 | TGCTTCCCCTGTGCT[G/T]CCAGGAAGTCCCCAC | 4215 |
| rs543710364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685221 | ATCTCCAGCGCCAGG[C/T]TCCAGTGTTAATGAG | 4215 |
| rs543831116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656584 | CACTCCAGCCTGGGC[A/G]ACAGAGTAAGACTCT | 4215 |
| rs543886307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627875 | AGGTGTGAGCCAATG[C/T]GCCCGGCCTGTCACT | 4215 |
| rs543946292 | snp | A/C/G/T | 0.000134845 | 0.00821009 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634659 | ATGTTGTCAAACTTA[A/C/G/T]GTTGCACGAAGGATA | 4215 |
| rs544019656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626076 | GAGAGACCCTGTCTC[C/T]AAAACAAAAAACAAA | 4215 |
| rs544035496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677209 | GATCATTTAGCTAAT[C/G]AGTGGCAAAGCCTGA | 4215 |
| rs544114717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632997 | TATTGGGAGGCCGAG[A/G]CAGGCGGATCACCTG | 4215 |
| rs544114951 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653641 | ACTAACTTACATTTG[A/C]TTAATTTAAAATCCC | 4215 |
| rs544186885 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690058 | AACCATGACTTCAGC[C/G]AATCCTCTGCTTCTT | 4215 |
| rs544249571 | snp | C/T | 0.000208344 | 0.0102043 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689495 | TTGTACGTTCCGCCT[C/T]GTAGCCTGGGGTGTG | 4215 |
| rs544316050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678873 | TGTCTCTACTAAAAA[C/T]ATAAGAATTAGCTGG | 4215 |
| rs544391579 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696338 | CAGTGCTTTCAGTTG[G/T]GGGGGGTGGAGGTAG | 4215 |
| rs544465033 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694655 | GCCCAGCCTTTGTTC[C/T]CCACTGGAGCAGAAG | 4215 |
| rs544473364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658629 | TCTTATGCTTGACAG[C/G]CTTTCCTTTTCTTTA | 4215 |
| rs544476122 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637236 | CCTAGGAGTCATAGA[A/G]TTGTTACTCATCTAT | 4215 |
| rs544527541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649169 | GGGCCAGGTACAGAG[A/G]CTCACGCCTGTAATC | 4215 |
| rs544530261 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694078 | CCCACCCTCGGGGAT[A/G]TGTCCTGACACTGCA | 4215 |
| rs544546803 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657117 | ATCCTCTGACCATCC[C/G]TCCACCCCTTCTCTT | 4215 |
| rs544581722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671304 | CTCTGTCACCAGGCC[A/G]AAGTGCAGTGGTGTG | 4215 |
| rs544601164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644462 | CTCCAGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 4215 |
| rs544631299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627709 | GGCCTCCCAAAGTGC[C/T]AGGATTACAGGCATG | 4215 |
| rs544694550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634578 | GGCAGAAGCCTAAAA[A/G]GGATTGACTGTTAGG | 4215 |
| rs544730161 | in-del | -/GAA | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648381 | TGTTGCTGAGGCCTT[-/GAA]GAAGGAGGGGTATGA | 4215 |
| rs544796905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651205 | AAACTTTTTATTGGC[A/C]AAGCATGGTGGCTTA | 4215 |
| rs544845811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665554 | TTTTGAATTCCCACT[A/G]TGTGTAAGGCCCTGC | 4215 |
| rs544965599 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696277 | AGGCCAGTGTTGCGC[A/G]TTACTTACAATAAAA | 4215 |
| rs545004124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627150 | CACAGGTTGGGGTAC[C/G]AGGAGAAGAAAAACT | 4215 |
| rs545052676 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674872 | TCAGGCAGAGGACAA[A/G]AAAGAATGTTGAAAG | 4215 |
| rs545066545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633916 | GGTTCCTAGAGATAG[C/T]ATAAGGCCCTAAAAC | 4215 |
| rs545094248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686290 | TAATTGTTCATTTGG[A/G]TAGTGATATTATGAC | 4215 |
| rs545172441 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669320 | CCAGGCTGGCTGATA[C/T]ATTTGGAGGAGGAAT | 4215 |
| rs545185203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665043 | CATGGTCGCTCACCC[C/T]TGTAATCCCAGCACT | 4215 |
| rs545191896 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693976 | CAGGACTGGGAGCCC[C/G]CAGCCTGTCAGATCC | 4215 |
| rs545198378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658547 | GTATCTGTCTTCCAA[G/T]TACTGATTCTTCTAC | 4215 |
| rs545223993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641096 | TACCATTTACCAACC[A/G]CTTGTATATCAGGTA | 4215 |
| rs545308192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671476 | GGCCAGGATGGTCTC[G/T]ATCTCTTGACCTTGT | 4215 |
| rs545431904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642668 | GTCTCAAAAAATAAA[A/T]AAATAAATAAAATGT | 4215 |
| rs545520106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650150 | TTGGGCATCTTTTCA[G/T]GTGTTTTATTAGCCA | 4215 |
| rs545573143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657605 | AGGTACTACAAATTT[C/T]TGGATTGTACATTTA | 4215 |
| rs545592584 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658377 | TTCAGTGGAAAAAGC[A/C]ATGGGTTGGGGGCCT | 4215 |
| rs545639002 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621379 | CAAAACAATACAAAG[C/G]CATTTTTGTCAAACG | 4215 |
| rs545692705 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689397 | TGCGGACGGGATGGG[C/G]TGGAGCTGGTATTAT | 4215 |
| rs545700684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629008 | CTTTATCTCCATTTT[A/G]CAGATGAGGAAATTG | 4215 |
| rs545722933 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680384 | GTTCAGGATAAGAGT[A/C]TTACGTTTAAGTTTT | 4215 |
| rs545789599 | snp | C/T | 0.000115419 | 0.00759581 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691194 | TCTGCGGGACCGCGC[C/T]GAGAAGACCCTGACC | 4215 |
| rs545805704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660471 | TTCTGTCTCAGCCTC[A/G]CAAAGTGCTGGGATT | 4215 |
| rs545825169 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630558 | TCTCGAACTCCTGGG[C/T]TCAAGCAATCCACCT | 4215 |
| rs545873849 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63622173 | AAACCGCCTTGGCTT[C/T]GCCCATTGGCATCCT | 4215 |
| rs545876324 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668517 | TTTGGCCTCTTTTCC[A/G]TAGTCCTTGTAGAGA | 4215 |
| rs545896313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674292 | TGGACCTGCCAGTTG[C/G]AGTGGTGCGTACCTG | 4215 |
| rs545931708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665816 | ATGTGATAAAGTCTG[A/G]CATGGGGACTACAGG | 4215 |
| rs545984347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682237 | TAACATACGACTGGT[C/T]CTAAAGTGACAGGTT | 4215 |
| rs546001243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673393 | TAGTTCATGCTAAAC[A/T]AAACAGAAACAAACA | 4215 |
| rs546095896 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695092 | TTGTCATTAAAGGAA[-/A]AAAAAAAAAAAAAAA | 4215 |
| rs546105176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636304 | AACAATTTTCTAGGA[G/T]GTAGATTCTGTATTC | 4215 |
| rs546122806 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624760 | CCTAGCTTTCTTCAC[-/T]TTTCCCCCATACAAT | 4215 |
| rs546159259 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675633 | AGCTGGCAGCTTAAA[C/T]CCCGCTTTTCTCCTT | 4215 |
| rs546176711 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650530 | CTAGTCTTGAACTCC[A/G/T]GACCTCAGGTGATCC | 4215 |
| rs546245657 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665431 | CAGCCTCCCAAAGTG[A/C]TGGGATTATAGGCAT | 4215 |
| rs546282270 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635932 | CAGTTGAAAGAAGCT[A/G]AGCATTTTGGCTAGC | 4215 |
| rs546340382 | snp | G/T | 0.000261499 | 0.0114316 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657951 | CTGAAGACAAAGCTT[G/T]CTTTCCTTCAGGAAC | 4215 |
| rs546387761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645294 | GGTGACAGAGTGACA[C/G]TCCGTCTCAAAAAAA | 4215 |
| rs546408505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627967 | CTGGAATGTGTTGGC[A/G]TAGTCTTGGCTCACT | 4215 |
| rs546447902 | snp | G/T | 1.66103e-05 | 0.00288182 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690270 | CTCCTGTAGCTCCCA[G/T]TGCCCCCATCAACTG | 4215 |
| rs546465782 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627426 | ACCTCAACTTGTTCA[C/T]GTGTAAAGTTCACAA | 4215 |
| rs546546205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661245 | AGAGATGGGGTTTCG[C/T]ACTGTTGGCGAGGCT | 4215 |
| rs546573812 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658844 | GCTTCAAATGATTCT[C/T]CTGCTTCAGCCTCTC | 4215 |
| rs546616337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634132 | TACACTATTTTCATA[C/T]GTTATTCAGTCTGAC | 4215 |
| rs546690563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672804 | GGTTGGTAAGGACAG[A/T]CCAAGGGTAAGAGAC | 4215 |
| rs546818521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628699 | CTTTGTATTTGTGTG[G/T]TGTTTATCTTTTTAT | 4215 |
| rs546851917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642835 | GATCATGGCTCACTG[A/C]AACCTCAAGCCCCCC | 4215 |
| rs546856183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671342 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAA | 4215 |
| rs546881804 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635808 | GCCAGAAAGTCCATG[A/C]TTAGGAAGAGAGAGG | 4215 |
| rs546945326 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632402 | GAGGCTGATGTGGGA[A/C]GGTCACTTGAGCCCC | 4215 |
| rs546971685 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695697 | GAGGATACAGAGCAC[A/G]GTGCTGGCTGACTCA | 4215 |
| rs546986573 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664726 | TCTATTTGTTGTCTT[C/T]AGAATGTTCTGCTAG | 4215 |
| rs546988345 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632356 | AATCATCCAGGCATG[C/G]TGGTGCATGCCTGTG | 4215 |
| rs547034600 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621640 | AGACAGGGAAAGCTG[A/G]GCTGGGCCGGCCGCC | 4215 |
| rs547108714 | snp | C/G | 1.77903e-05 | 0.00298242 | missense, downstream-variant-500B, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681886 | AGTTCATCCCAGAGA[C/G]CAGCGAGCAGTGCGT | 4215 |
| rs547109246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636650 | GGGACACAGCCACGC[A/C]GATCCAGCATGTGTC | 4215 |
| rs547149711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637083 | AGAGCGTGTGTAGAG[G/T]GTCGATGTTGCAGCT | 4215 |
| rs547164009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690534 | TTCTTCCCAAACTCC[C/T]TTTCTGTCCATCCTG | 4215 |
| rs547278050 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629121 | AGTCTAAGAAAGTTG[C/T]TATTTGTTGTTTTTT | 4215 |
| rs547337401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682610 | AGTTTTTTTGTGGCT[A/G]TAGGACTGTGGTTCC | 4215 |
| rs547371404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637696 | ATGGGATTATCATTA[C/G]TGTTTATCTGATGAT | 4215 |
| rs547385171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646890 | ATGTGCCTTTCGGTG[G/T]TTTTTCCACTCTTTG | 4215 |
| rs547619925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660792 | GTAGAGACGGAGTTT[C/T]TCCATGTTGGTCAGG | 4215 |
| rs547636022 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649536 | GCAGTCCTCCTGCCT[C/G]AACCTCCCAGGTGCC | 4215 |
| rs547654341 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642431 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACTTGAG | 4215 |
| rs547677292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652216 | CCCCAGTGTGTATTG[C/T]TCCCCCTCCATGTGT | 4215 |
| rs547683975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666761 | AAAACTACATTGAGC[A/G]AATAGTGGTTTGCTG | 4215 |
| rs547691007 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636786 | CAAGGAGGCAGCCCG[C/G]CTGTGGGAGAAGTGG | 4215 |
| rs547882043 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636784 | GACAAGGAGGCAGCC[C/T]GGCTGTGGGAGAAGT | 4215 |
| rs547923441 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662701 | CTCACTCTGTCACCC[A/C]GGTTGGAGTGCAGTG | 4215 |
| rs547944042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643856 | ACTGTTTAGAATTTC[A/T]GGGGAACGAGAAAAA | 4215 |
| rs547985652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668613 | GGTCTCTTGCCCCCA[A/G]GCAAGAGCCTATGAT | 4215 |
| rs548048628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675733 | TGCTTCAGCTGGTGG[C/T]ACAGGTGGCGCAGTG | 4215 |
| rs548109228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631349 | GCAGTTTTACTTCCT[A/G]CATTTCATGCTGTTC | 4215 |
| rs548118381 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650568 | GCAGCCTCCCAAAGC[A/G]CTGGGATTACAGGCA | 4215 |
| rs548119424 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630141 | ACACTTAAACCTAGT[C/G]ATAATCCTCCTTGTA | 4215 |
| rs548167940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653592 | GTTCATACATGTCTT[A/T]ACATACTCTACTAAT | 4215 |
| rs548173754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644880 | GACTATGACTTCATT[A/C]TCTCCTTTATCTCTA | 4215 |
| rs548177483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690483 | CTTACCACACAGAGT[A/T]GTTGCCTGAGATGCT | 4215 |
| rs548207933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665323 | GGTGCCTGCCACCAC[A/G]CCCAGCTAATTTTTT | 4215 |
| rs548237194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661644 | TTACCTCATATTCGC[A/G]TTGACAAAAATAAGC | 4215 |
| rs548274436 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652671 | GGTGAGAAGGCAGAT[C/G]GATGGGGCAGGGACA | 4215 |
| rs548287042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662039 | ACCCAGGAGGCGGAG[A/C]TTGCAGTGAGCCAGG | 4215 |
| rs548303450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667411 | TGTAAAGTTAGGAAT[A/C]GGGTCTAAGTTTGAA | 4215 |
| rs548388775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622922 | CGCCCGCCCCGCTCG[C/T]GCGCCGCGGCCCGGG | 4215 |
| rs548390636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631214 | TTGTTTGAGCCTGGG[A/G]GTGGAGGAGGCTGCA | 4215 |
| rs548451868 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630152 | TAGTCATAATCCTCC[C/T]TGTATTGATCCCAAT | 4215 |
| rs548463057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659137 | TTAGCCTTGCAAAGT[A/G]CTGGGATTACAAGTG | 4215 |
| rs548549598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674545 | GTAGAGATGAGTTCT[C/T]ACTATGTTGCCCAGC | 4215 |
| rs548555275 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626929 | AGAGAGAGTGTGTGG[C/T]ATAGTAAACAGACAC | 4215 |
| rs548616306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676798 | CACACCTGTCAACAT[C/T]GGCAAAGCTGGAGAC | 4215 |
| rs548636225 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659117 | GCTCAAATGATCCAC[C/T]CACTTTAGCCTTGCA | 4215 |
| rs548677331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684385 | CTGATGGATTTAAAG[C/T]AATTCTCTCCGATGT | 4215 |
| rs548677696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675836 | GCCTTCTGAGACCTA[C/T]GGAATGAGCTGTTTT | 4215 |
| rs548734462 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675146 | TGGGAATTTTGAAAG[C/T]TGAAACATAGAAGAT | 4215 |
| rs548738540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683653 | ATTGCTCCTGGTAAC[A/G]GGCCATTTGAGATCA | 4215 |
| rs548827601 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677740 | GTGGATGTGGCTCAC[A/G]CCTGTAATCCCTGCA | 4215 |
| rs548844290 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682515 | GTCACACAAGACTGC[A/C/G]ATCAAGGTGTCAGCC | 4215 |
| rs548877607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692828 | GAGAGCTTCTCCCCT[G/T]GGAAAGCTATTGTGG | 4215 |
| rs548910882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681732 | GCCACACACCCTGGG[C/G]TCTGTTGTTGAAAGC | 4215 |
| rs548948895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669704 | ATGACCACCTGCCTC[A/G]GCCTCCCAAAGTGTT | 4215 |
| rs548995630 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638793 | GGCTCATGCCTGTAA[C/T]CCCAACACTTTGGGA | 4215 |
| rs549017265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625664 | GACCACCTATGTAGA[C/T]TCTGAATAGTTAGCA | 4215 |
| rs549035028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645978 | GCTTACTTGGCAATG[A/G]CAGGAGTGACACATT | 4215 |
| rs549038154 | snp | A/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682882 | AGGGAAAGGCAGTTC[A/T]TTGGGACTAATTGGA | 4215 |
| rs549073602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686585 | GGACTACAGAAGGTC[C/T]AGTAGTTGGGAAATG | 4215 |
| rs549080632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624926 | TTCACACACAGTCTC[G/T]CTCTTAAATACTAGT | 4215 |
| rs549110514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641203 | TTTACAGATGAGGAA[A/G]CTAAGTTATAGGTTA | 4215 |
| rs549165933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638726 | GTTTAACATGTGCCT[A/G]TGGTCACGCTTCTCA | 4215 |
| rs549225556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646849 | GACCTTGCATGTTTG[C/T]GCATGTGCGGCACAT | 4215 |
| rs549225643 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653562 | AGCCAAATATAAATC[A/G]TTGTTATTATTTTAG | 4215 |
| rs549371897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663228 | CAATGCTTGGCCAGG[C/T]GTGGTGGCTCATGCC | 4215 |
| rs549421788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640223 | AGCTCAAATCTGTAG[C/T]GCACAGTGATTGTGC | 4215 |
| rs549427773 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646858 | TGTTTGTGCATGTGC[A/G]GCACATGTACACATA | 4215 |
| rs549436656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670314 | TGGGCTGGGCATGGT[C/G]GCTCACGCCTGTAAC | 4215 |
| rs549447984 | snp | C/T | 3.31093e-05 | 0.00406861 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693700 | CGGGACTTCCTGAGG[C/T]GCATTTTTGTGGAGG | 4215 |
| rs549464059 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649270 | GGTGAAACCCTGTCT[C/G]TACTAAAAATATAAA | 4215 |
| rs549475086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692112 | GCTAAATCCTTTGCC[C/T]TTTGCAGTTCATGTC | 4215 |
| rs549483252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665097 | CACCTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 4215 |
| rs549538320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691433 | GGAGTATGAGATGAC[A/T]GCTGTCCTAGGTCCA | 4215 |
| rs549557470 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675382 | GTGACCTGCACATTA[A/T]CACTGACCCAAAGCC | 4215 |
| rs549643373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646615 | AAAGAGGGAGTTTTT[C/T]GGTCTGTGTTCTGAA | 4215 |
| rs549675173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662857 | GAGATGGGGTTGGGC[A/G]GGGGGCGGTCCTCAC | 4215 |
| rs549734072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675797 | AAAGGTGTCCCAAGA[A/G]AGCCTGTGACCCCTG | 4215 |
| rs549808497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631827 | GGAAGTAGTAGGCCT[A/G]TAAACTTGTAAAGAG | 4215 |
| rs549827537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652889 | TTCAGTGCAGATAGC[G/T]CTAATATTCCATGGT | 4215 |
| rs549837596 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652493 | AATATACTCAGACCA[C/T]TGCTTTTTAAACCCT | 4215 |
| rs549838959 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644947 | TCCTCTACACCTGTT[C/T]TTCTGTAATATCTCT | 4215 |
| rs549901391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648555 | TCTGGGCCGGGTGTG[A/G]TGGCTCACGCCTGTA | 4215 |
| rs549942772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645856 | CCTGATGTTAGAACT[A/G]GAAGTTTTAACTCAT | 4215 |
| rs550007122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653534 | AAGAATTCCTGATGT[A/T]TCTTTATTCTAAAGC | 4215 |
| rs550073656 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642198 | TTAGTCACAGGCTTG[G/T]TTAGTCTTAAGTAGC | 4215 |
| rs550155653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664550 | ATAATTTGTGGGTGG[A/G]CTTTTGTAACTTATT | 4215 |
| rs550165530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669594 | CTGCCTCAGCCTGTT[A/G]CAGGTGCACACCACC | 4215 |
| rs550188210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625479 | ACTGAAAAATATGTA[A/T]CAACTTGGAAATGCT | 4215 |
| rs550205487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647783 | TCTAGTTTCGTGTAT[C/T]TCACGTCAGGATTTT | 4215 |
| rs550260410 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686763 | GTTTTTTCCTCTGTG[C/T]CTGCAGTACTTTGTT | 4215 |
| rs550272143 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663994 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 4215 |
| rs550306980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627276 | TGAATACTCCTCCTT[C/T]TCCTAGATTCTTAAC | 4215 |
| rs550370337 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626474 | TGATATATATTGATT[C/G]TTATGAGGAATAAAT | 4215 |
| rs550370436 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634092 | CTTATAGTACTGGAG[G/T]TATAAACAGATAAGG | 4215 |
| rs550391622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662750 | GCAGCCTCCATCTCC[C/T]GGGTTCAAGCGATTC | 4215 |
| rs550424789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671329 | GGTGTGATCTCGGCT[C/T]ACTGCAACCTCCGCC | 4215 |
| rs550454846 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662176 | TTTGGGAGGCTGAGG[C/G]AGGCAGATTACTTGA | 4215 |
| rs550484065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678168 | GGGGCTTGGGTTTCC[C/T]TCTGCGCAATGTGGA | 4215 |
| rs550543796 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634534 | TGTGCCTGCTGCTGC[A/G]CTGGTAGAGTGAAGT | 4215 |
| rs550671676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679245 | CAGAGCAAGCCTCCC[C/T]GCCATTCTTTTTTTC | 4215 |
| rs550796727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677580 | GTGGAGTAGTTCCCT[C/T]GGTCCAGATTTCCCC | 4215 |
| rs550899723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642176 | GCATCTTTGTTTACA[C/T]TGCTTTTTAGTCACA | 4215 |
| rs550926327 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694854 | AGCTCTGTTCTTCCT[C/G]AGCCAGCCTCGCCCA | 4215 |
| rs550941277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663370 | AGCTGAGCGTGGTGG[C/T]GCATGCCCGCAATCC | 4215 |
| rs550961122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650338 | AGAGTCTCTTGCTCT[G/T]TTGCCCAGGCTGGAG | 4215 |
| rs551003199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628579 | TGGTCAGGCTGTTCT[C/T]GAACCCCTAACCTCA | 4215 |
| rs551026960 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638330 | AAATGCAGGGAGAGA[A/T]ATCAGTACAGAATCA | 4215 |
| rs551063934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634246 | CCCTTGCTTGAGCCT[A/G]ATGACCTCACTTTCC | 4215 |
| rs551066190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635736 | ATTATTATTGTAGTT[G/T]TTGTTAGCCTAGGCC | 4215 |
| rs551067760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669800 | TACGTTTTTGTTCAT[C/T]CATTCAAAAGATAAT | 4215 |
| rs551097397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642748 | TCGTTTTTTTGTTTT[A/G]TTTTGTTTTGTTTCA | 4215 |
| rs551129170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676959 | ATACAGCTTTTAGCC[A/G]GTTAGCTTCTCAAGT | 4215 |
| rs551137783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635190 | ATGACTTTATGCACT[A/G]TGTAAGGGACTGTTG | 4215 |
| rs551173491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626383 | GAGATCAATTCTGTC[A/G]TTTTGGTATTGACAC | 4215 |
| rs551190340 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670337 | CCTGTAACCCCAGCA[C/T]TTGGTGAGGCCGAGG | 4215 |
| rs551235172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633121 | TAGTCCCAGCTACTC[A/G]GGAAGCTGAGACAGG | 4215 |
| rs551236212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639325 | ATGATTAAAGGCCTA[G/T]GGGAAGAAGCAAACA | 4215 |
| rs551249551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685773 | AAATGAATGTAATAA[C/T]AGCTCATAAAATAGC | 4215 |
| rs551395245 | in-del | -/TT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667467 | GATTCCTGAGAAGTC[-/TT]TATACTTCAGGGAAG | 4215 |
| rs551452522 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694758 | TCAGGCTGCCTGAGT[C/T]GTGACCTGCTAGGCC | 4215 |
| rs551501435 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625870 | TGAGCCCAGGAGTTC[A/G]AGAGCAGCCTGGGCA | 4215 |
| rs551512374 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694199 | TCCTTCCAATGTCTG[A/C/G]AGACCACCAGGGCAT | 4215 |
| rs551562207 | snp | A/G | 3.30142e-05 | 0.00406276 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632683 | TCTTTCATTGCAGAC[A/G]AACAGGAGGCATTGA | 4215 |
| rs551578531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684599 | AATTTTATGGAGGTC[A/G]TTAGTGAATTTTCAT | 4215 |
| rs551646151 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628362 | TTGTCTAATTCTGTC[-/T]TTTTTTTTTTTTTTT | 4215 |
| rs551678874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649343 | TCGGGAGGCTGAGGC[A/G]GGAGAATGGCATGAA | 4215 |
| rs551689268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692948 | TAGGATTAGGTTAAG[A/G]GTTTTGAGATGGATG | 4215 |
| rs551810627 | snp | C/T | 0.000198331 | 0.00995621 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634851 | TACTTTTAAATCTGC[C/T]ACTCATGCTGCAACA | 4215 |
| rs551830133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675742 | TGGTGGCACAGGTGG[C/T]GCAGTGAGGCTAGAG | 4215 |
| rs551842378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687026 | GTGAAAGAAAGATGC[C/T]TGGTTTAGCAGCAAG | 4215 |
| rs551944344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651345 | AAATTAGTCGGTGCA[C/T]GCCAGTAGTCCCAGC | 4215 |
| rs551954811 | snp | A/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621381 | AAACAATACAAAGCC[A/G]TTTTTGTCAAACGCC | 4215 |
| rs552196191 | snp | C/T | 3.29462e-05 | 0.00405857 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666908 | CTGACTGTGTAAAGA[C/T]GTAGCTTGGCCTTTT | 4215 |
| rs552378917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665235 | CAGTGGTGCGATCTC[G/T]GCTCACTGCAAGCTC | 4215 |
| rs552444220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664717 | ACACCATCTTCTATT[C/T]GTTGTCTTTAGAATG | 4215 |
| rs552444292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672540 | GTCTCTAGCTCAGAG[A/G]GGAGAAAATCAGGGC | 4215 |
| rs552461995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673911 | TGGTCTGTCTCAAAA[A/G]AATAAAAAATAAATA | 4215 |
| rs552502978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629267 | AGCTGGGATTACAGG[C/T]GCACACCACCACGCG | 4215 |
| rs552504231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671639 | CCAGAGGTCAGGTGC[C/T]TGAGGTGATGTCATC | 4215 |
| rs552541700 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680803 | TTTTGGGTGTTTTGG[G/T]TTTTTTTTTTTTTTA | 4215 |
| rs552622103 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622689 | TCCCCGCCGCCCGGG[C/T]CCCCGGCATGCAGCC | 4215 |
| rs552640021 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628944 | CATAAGAAATAATTC[A/G]TAGGTTTTCTGTTGC | 4215 |
| rs552649773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687187 | CCTGACCAGCATAGC[A/G]AAACCCCGTCTCTAC | 4215 |
| rs552675461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648800 | AGCCTGGGGGACAGA[A/G]CGAGACTCCATCACA | 4215 |
| rs552705492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681608 | ATTAGGAAGGGACTT[C/T]GTTTGCCTGAGGGAG | 4215 |
| rs552737586 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654398 | TTGTCAGTATGTCAT[A/T]CTATTTTATGGCTGA | 4215 |
| rs552773896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696603 | CAGTGGCTGAGTTCC[C/T]GGAGCTTTCATGATA | 4215 |
| rs552877142 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627091 | GAAGAGTGGCTTCCT[A/G]CTGGAGCTAAAGAGA | 4215 |
| rs552929655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663484 | TCCAGCCTGGGCGAT[A/G]AGCGAAACTCCGTCT | 4215 |
| rs552974409 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689748 | AGTGTGAGGAGCTGT[C/T]CCTGGCTAGGAGGAG | 4215 |
| rs552994954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670815 | GAAAGAAGTCCAGAT[A/T]GCTGGAGAGCTGGGA | 4215 |
| rs553045116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656984 | AAGGGGGAAAAGCTC[C/T]GTGAGAATGGAGGAG | 4215 |
| rs553072927 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625414 | TGTTCATAATACCTG[A/G]GATTGTTTATGTGGT | 4215 |
| rs553097701 | in-del | -/TG | 0.0103295 | 0.0711199 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634148 | GTTATTCAGTCTGAC[-/TG]TGTGAGTTCTCCCTT | 4215 |
| rs553110881 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644353 | CGAGTAGCTGGGATT[-/A]ACAGGTGTGCGCCAT | 4215 |
| rs553114959 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671985 | GACCCAATATCATTT[A/T]AAAAAAAAAAAATGA | 4215 |
| rs553120834 | snp | C/G | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681286 | GGGAACAGGGCAACA[C/G]AGAGAGATGCACAGG | 4215 |
| rs553195043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665001 | TTCTGTTGATCTGAG[A/G]TGTCAAAATCTCCAC | 4215 |
| rs553239659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678536 | TTGCTCTGGAGTCAG[A/G]TGGGGAGGCCAGATT | 4215 |
| rs553372153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665401 | TGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 4215 |
| rs553389215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650848 | AAGCATGTACTATCA[C/T]ACCTGGCTAATTTTT | 4215 |
| rs553533726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628122 | TGTTGACCAGGCTGG[C/T]CTTGAACTCCTGACC | 4215 |
| rs553564523 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696809 | TGCCCTGAGAGGCTC[A/T]GAGGCGCTCACTTCA | 4215 |
| rs553626366 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696109 | GGGCTGGGGACAGTC[C/T]GCACTCTGCCACCCT | 4215 |
| rs553640579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680368 | TCAGAACAGGAAAAG[A/G]GTTCAGGATAAGAGT | 4215 |
| rs553668464 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627622 | TAATTTTGTATTTTT[A/T]GTAGAGACAGGGTTT | 4215 |
| rs553697672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689191 | CTGTAGAGGGGTAAG[A/G]AGTAGGATACAAGGA | 4215 |
| rs553749241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638105 | TTTGAAAATAAGATA[A/T]AAAACAACACACAAG | 4215 |
| rs553768817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666488 | ATCAGTCAATAAGAT[A/G]AATACATATATAGCA | 4215 |
| rs553770695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674607 | TTCTACACCTCAGCT[G/T]CCCAAAGTGCTGAGA | 4215 |
| rs553813257 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677670 | CCTGGCCTCTGACTC[C/T]CAAATGACCATGGAG | 4215 |
| rs553825104 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681215 | CTGGCCAGACCATCA[C/T]GAAGGCCTTTTTACC | 4215 |
| rs553952097 | snp | C/T | 0.00483431 | 0.0489263 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691044 | GCAAGCTGAGCTGAA[C/T]CCAGGCGGGCAGAAC | 4215 |
| rs553988954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653748 | GATTTTATTTATTTA[C/T]CTCTTTGTAATTATA | 4215 |
| rs554009749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644133 | TGGTTTGTGGTAAAT[A/G]CTCAATAAACGTTAG | 4215 |
| rs554027888 | in-del | -/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680582 | TTGGGCTAGGAGGAA[-/G]GGAGGACCTGATTTC | 4215 |
| rs554090241 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623302 | GGGAGGGCGTGCGGG[C/G]CTCGGCTAGGAGGCG | 4215 |
| rs554152025 | snp | C/T | 8.31635e-05 | 0.00644786 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691719 | GGACTCCTCTGACTT[C/T]TTGTGGCCTCCAGGG | 4215 |
| rs554173221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660431 | TTGCCCAAGCTGGTC[G/T]CAAACTCCTGGGCTC | 4215 |
| rs554187541 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647972 | ACTTTCCCTTTACTT[A/T]GAGAATATGGGGACC | 4215 |
| rs554240891 | snp | C/T | 0 | 0 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673066 | GAATATTTAGTGAGT[C/T]TGCAGCAAGCAGGCT | 4215 |
| rs554384832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661201 | ACAGGTGCATGCCAC[C/G]ATGCCCGGCTAAGTT | 4215 |
| rs554457415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642529 | CAGGCATGGTGGTGC[A/G]TGCCTGTAATCCCAG | 4215 |
| rs554466425 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684203 | TCCCTGCTTGACTTC[C/T]AACCATAAAGAACGT | 4215 |
| rs554484166 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695335 | CATATTTGATGGTTT[A/T]TATATATATCAATTC | 4215 |
| rs554510109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667138 | CAAGTATTTGTTAAT[C/T]AAATAATCATCAAAT | 4215 |
| rs554666486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660935 | GCAGCTTCTAATTTT[C/T]CTTCTGTCTTCATTC | 4215 |
| rs554679157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642963 | GCGTTTTGCCATGTC[A/G]CCCAGACTGATCTCA | 4215 |
| rs554700906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688954 | GGGGAGGGTGGGTTC[A/G]TCCATGCAGTGCCTG | 4215 |
| rs554729342 | snp | A/G | 1.79596e-05 | 0.00299658 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63681772 | GTGCTCTAGGCTCCC[A/G]GAACCCTGGCCGAAG | 4215 |
| rs554729762 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660379 | TGGCTTTTCTTTTTT[C/T]TTTTTTAATTGTTTG | 4215 |
| rs554758061 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687893 | CGGTGAGCTGAGATG[C/G]TACAGCACTCCAGCC | 4215 |
| rs554794827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651409 | GCCCCAGAGGTTGAA[A/G]CTGCAGTGAGCCGTT | 4215 |
| rs554857921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650814 | CTCCCACCTCAGCCT[C/T]CCAAGTAGCTTAGAC | 4215 |
| rs554881016 | snp | A/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621203 | CATTAATTGTGGTGG[A/T]CTTGGAATCTGAAGA | 4215 |
| rs554885358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629342 | GTTGGCCAGGCTGGT[C/T]TCGAACTCCTGACCT | 4215 |
| rs554909850 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641690 | ATTGGCCTCAGATAC[A/G]TGGCAAGCAGATGAG | 4215 |
| rs554912647 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651453 | CACTCCAGCCTAGGT[A/G]ACAGAACGAGACTCT | 4215 |
| rs555170021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674777 | TGCTGGAGATGAATC[A/G]AGTCCAGGTAGAGGG | 4215 |
| rs555171606 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682801 | CATAATCATAGGAAT[A/G]AATATTCTATCCTCT | 4215 |
| rs555193528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666344 | CTACTTTTAAACATA[A/C]ATATATAAGCTGGGC | 4215 |
| rs555209551 | snp | A/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621041 | AAAAGAAATAGGGGA[A/G]AGCCCAAGGTAATTC | 4215 |
| rs555337367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638074 | TCAAGGGTTGTTGAT[A/G]AGATGGGCTGGCCAG | 4215 |
| rs555343606 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634925 | AAAGCATTGGTTACC[C/T]GTGACCTGTGTTCAG | 4215 |
| rs555343831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625998 | AGATCATCTGAGCCT[C/G]GGAGGTTGAGGCTGC | 4215 |
| rs555365937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691546 | GGATTTGGGTGGCGC[C/T]CTGCTTGAGAAGGAC | 4215 |
| rs555380548 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667928 | GTCCTTCCCAGGACA[A/G]GAATCTAAATCAGGC | 4215 |
| rs555387096 | snp | G/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675992 | CATTGGCTCCCAATT[G/T]CTGAAATGAAGATTA | 4215 |
| rs555389939 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653916 | CTGTCGCCCATGCTG[G/T]AGTGCAGTGGTGCAA | 4215 |
| rs555442543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668061 | GGAAATCTGGTCTTA[C/T]CAAACATCGTGTTGA | 4215 |
| rs555544824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624104 | GCGTGCTCTTCTGAG[A/G]GAAGGTCTGCTGTGA | 4215 |
| rs555588888 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642818 | CTGGAGTCCAGTGGC[A/G]TGATCATGGCTCACT | 4215 |
| rs555626894 | snp | A/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673989 | GGAGGCTGAGGTGGG[A/T]CAATCACTTGAACCC | 4215 |
| rs555638540 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630566 | TCCTGGGCTCAAGCA[A/G]TCCACCTGCCTCAGC | 4215 |
| rs555762978 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677841 | CCACTGCACTCCAAA[G/T]AAAGAAAGATACATG | 4215 |
| rs555774091 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660000 | TTTCTTTACTTACTT[-/G]GTGGAAGAGCAGGAC | 4215 |
| rs555858105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632289 | TGGAGTCCAGGAGTT[A/G]GAGACCAGCCTGGGC | 4215 |
| rs555944158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692630 | GCTGGGAACTTAGGC[C/T]ATGGAAAACATCCCT | 4215 |
| rs555977286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690736 | GCTCTCAGCCCAGGA[A/G]GGAGCTGTGGGGCTC | 4215 |
| rs556020936 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63622189 | GCCCATTGGCATCCT[G/T]TGAGAGTAGGCGGGA | 4215 |
| rs556038664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690023 | AAGGAAATGCATTTG[A/G]TCAATGCAGAAGAGC | 4215 |
| rs556046989 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647105 | CCTACTTTGCAGCTG[G/T]CTCCAGAGGAGACCT | 4215 |
| rs556117078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681285 | GGGGAACAGGGCAAC[A/G]GAGAGAGATGCACAG | 4215 |
| rs556120558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654657 | TATAATGGTTGCACA[A/G]TTTTACAGTCCCACT | 4215 |
| rs556176970 | in-del | -/CAGTTAGGCTCTC | 0.00358779 | 0.0422022 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647441 | TGGAGCCCAATTACG[-/CAGTTAGGCTCTC]CTGAATTCCCTGTTC | 4215 |
| rs556178192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661293 | CTCAAGTGATCCGCA[C/T]GCCTCAGCTTCTCAA | 4215 |
| rs556230600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674708 | GAGGGATAAAGACAG[C/G]TGAAAAGGAGGGGTT | 4215 |
| rs556240867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667215 | TTTATTTAGAGAGGA[A/G]GGGCAAAGAAATAAC | 4215 |
| rs556267098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638191 | CCTACAACTTTCCAG[A/G]GTCATGCTTAAAAAT | 4215 |
| rs556389608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637144 | GTGCGTGCATGCGCA[C/T]GTGTGCAAGTGTGTG | 4215 |
| rs556413536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647048 | CTTAGTACCTCTAAA[C/T]ATTCTTGATTCTGGT | 4215 |
| rs556441491 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644375 | GTGCGCCATTACTCA[C/T]GGCACACTTTTTGTA | 4215 |
| rs556587454 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661772 | GGAAGATAAAACAAA[C/T]CTGATTGGGCAGAAT | 4215 |
| rs556659653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655741 | TCAAGTGAGCCTCCC[A/G]CCACAGCCTCCTAGG | 4215 |
| rs556659824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663427 | GAATTGCTTGAACCT[A/G]GGAGGCGGAGGTTGC | 4215 |
| rs556709554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646312 | TTACTGTTCTGCTCT[A/G]TTCTGCTGCTGTGAG | 4215 |
| rs556721048 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662921 | TTCAAATGATCTGAC[C/T]GCCTTGGCCTCCCAA | 4215 |
| rs556770021 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630162 | CCTCCTTGTATTGAT[C/G]CCAATTTATTATTAC | 4215 |
| rs556774609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653865 | GCTATCTAATTCCAG[A/G]ACATTTTCTTTTTTT | 4215 |
| rs556916143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661896 | ATCACAAGGTCAGGA[G/T]ATGGAGACCATCCTG | 4215 |
| rs556921186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669975 | AAGTGTGGTGGTGCA[A/G]GCTTGTAGTCCCAGG | 4215 |
| rs556944355 | in-del | -/AGC | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685786 | AATAGCTCATAAAAT[-/AGC]AGCTCATTTATTAAG | 4215 |
| rs556947605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625946 | GGCGTAGTGGCATGC[C/T]CCTATAGTCCCAGTT | 4215 |
| rs556970927 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648201 | GAAGTCCTGGCCTCT[G/T]ATCTTGACCAGACTT | 4215 |
| rs556982263 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676989 | TACAGGAAGGCACAG[C/T]AGAAGGGTGGAATCC | 4215 |
| rs557130264 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687596 | TTGGGAGGCTGAGGC[A/C]GGAGAATAGCTTGAA | 4215 |
| rs557164690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687154 | GCGGATCACCTGAGG[C/T]CAGGAGTTTGAGACC | 4215 |
| rs557187974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671402 | CTGGGACTACAGGCA[C/T]GCGCCACCACACCCA | 4215 |
| rs557233612 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669152 | CAAGAAATGGGAGAG[A/G]TGATTTCTAACTGGA | 4215 |
| rs557398535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640425 | TGTGTATGTGTGTAC[A/G]TTGATTTTTGCAGGT | 4215 |
| rs557438634 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664076 | TGAAACCCCATCTCT[A/T]CTAAAAATACAAAAA | 4215 |
| rs557467192 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668320 | TAACTTCTGGAATCC[A/G]GGCAAGTACTGGTAG | 4215 |
| rs557503852 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665301 | CTCCTGAGTAGCTGG[C/G]ACTACAGGTGCCTGC | 4215 |
| rs557510945 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662883 | CTCACCATGTTGGCC[A/G]GGCTGGTCTCGAACT | 4215 |
| rs557532415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627521 | GATCTCAGTTCACTG[C/T]AACCTCTGCCTCCCG | 4215 |
| rs557559405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668257 | TATGCCTCCTGAGGG[A/G]GTTACAGGAAAAATA | 4215 |
| rs557588200 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641462 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 4215 |
| rs557591654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634392 | TGAATTGGAAGGCCC[A/G]AAAGGACGAGGCTGG | 4215 |
| rs557593463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626912 | TTGTATCTATGGAAA[A/G]GAGAGAGAGTGTGTG | 4215 |
| rs557622580 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675519 | GAGTACAAAGCAAAA[G/T]AACCTACCATATCCG | 4215 |
| rs557647190 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662098 | ACAGAGCGAGACTCC[A/G]TCTCATCTCAATAAT | 4215 |
| rs557756588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683861 | GCCTAATTTTTCCAA[C/T]AAAAATTATGTCAGT | 4215 |
| rs557768032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650304 | CAATCAGAAGTTTAT[G/T]TATTTATTTTTTTGA | 4215 |
| rs557776313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654833 | ACGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 4215 |
| rs557837788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662288 | CCAGGTGTGGTGCGT[A/G]CCTGTGGTCTTAGCT | 4215 |
| rs558094450 | in-del | -/TTCTTC | 0.0138799 | 0.0821421 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660566 | TTTCTTCTCTTTGGA[-/TTCTTC]TTCTTCTTCTTCTTC | 4215 |
| rs558189191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634644 | CCATGATTTACTTCA[A/G]TGTTGTCAAACTTAT | 4215 |
| rs558189242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642390 | CCAGGGCTGGGGCAG[C/T]GGCTCACACCTGTAG | 4215 |
| rs558213187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671029 | TGGATAACAGATTGG[A/G]GGGGGCAAGAATGCA | 4215 |
| rs558250512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641683 | ACTACATATTGGCCT[C/G]AGATACGTGGCAAGC | 4215 |
| rs558262596 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639985 | GAGAATGGGAAGCAG[A/C]GTCTTATACCGGAGG | 4215 |
| rs558301172 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635936 | TGAAAGAAGCTAAGC[A/G]TTTTGGCTAGCTGGA | 4215 |
| rs558302727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677127 | CACATTTATAACTTC[C/T]GAAAGAAATTATGAG | 4215 |
| rs558450090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639617 | CTGAAATGTATCCTC[A/G]CTCTGATTCTGTACT | 4215 |
| rs558456393 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645214 | AGGCCGAGGCAAGAG[A/C]ATCGTTTGAACCCGG | 4215 |
| rs558514160 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657024 | AGGTTCTAGTCACTG[A/G]CTTTGCCCTTAAACA | 4215 |
| rs558548531 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696303 | TAAAAGGGATCATTT[A/T]TATCAGAGGGGTCCT | 4215 |
| rs558550351 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672771 | GTGTGGGGAGAAGGC[A/T]TTACACAGAACCAGC | 4215 |
| rs558570599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660297 | CCTCAACCTCCCAGA[C/G]TCAAGTTATCTTCCT | 4215 |
| rs558621860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687808 | TCTTGGCCAGTGGCG[C/T]GTGCCTGTAGTCCCA | 4215 |
| rs558645159 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659640 | CGGGTTCAAGCAATT[A/C]TTCTGCCTCAGCCTC | 4215 |
| rs558680161 | snp | C/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675030 | AAACAAAATGGTTAG[C/G]TTCTTTCATCTTCAA | 4215 |
| rs558683342 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695225 | TTCGTTGTATGTTGA[C/T]GATGCACTTTTATGA | 4215 |
| rs558746859 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694507 | CTGTTTTACAAGTTG[G/T]AGTCACTCTTATGCT | 4215 |
| rs558774221 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695255 | AATGTAGTTTCTATC[A/G]CTGTTTTTAGCCTTT | 4215 |
| rs558819852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656553 | GACATTGCAGCAAGT[A/T]GTGATTGTGCCACTG | 4215 |
| rs558833286 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672103 | ACCTGACCAACATGG[C/T]GAAACCCCGTCTCTA | 4215 |
| rs558879225 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677895 | CAGGAAGTCCCCACG[G/T]TAGCCTCCCTCCCAC | 4215 |
| rs558897831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664024 | GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 4215 |
| rs558923363 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666094 | TTCTCAGTGCAAAGG[A/C]CCCCCTTTGTTGCTT | 4215 |
| rs559118632 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620931 | GAATTGCTTGAACAC[A/G]GGAGACGGAGGTTGC | 4215 |
| rs559125344 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627944 | GAGTCTCTACTCTGT[C/T]GCCCAGGCTGGAATG | 4215 |
| rs559150951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672955 | TCCTAGCAGTAGAAA[C/T]GGGGTCCAAGAAGTC | 4215 |
| rs559160817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655885 | CAATATAATATGATT[A/T]GCAGAACATTCTCCC | 4215 |
| rs559170809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647494 | ATGCAGTTACAGTGA[A/G]CAGGCTTACACTGAG | 4215 |
| rs559211386 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680086 | GGTCTCCAGCTACCA[A/C/G]ACTTGGTCTCTCTTG | 4215 |
| rs559224602 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655014 | TTTGAGACAGAGTTG[A/C]GACTCTGTCTCAAAA | 4215 |
| rs559241570 | snp | G/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621540 | CTCTGGCGGAACTCA[G/T]ATTTCCAGGGACCCA | 4215 |
| rs559254240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630579 | CAATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 4215 |
| rs559283401 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648319 | GTGCTAGGGACATCT[G/T]AGTGGACTTCTGGTA | 4215 |
| rs559304209 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624432 | CCAGTTAGAGTGCCC[A/G]CATGTGTTGACTACA | 4215 |
| rs559365426 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629280 | GGCGCACACCACCAC[A/G]CGCAGTTAATTTTTT | 4215 |
| rs559388758 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666893 | AAGACCTTGATAGGC[C/G]TGACTGTGTAAAGAT | 4215 |
| rs559409118 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649853 | CTGTTACAGAAGAAC[A/G]TTAAAGAAATTATCT | 4215 |
| rs559611090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671285 | TTTTTGTGACGGAGT[C/G]TTGCTCTGTCACCAG | 4215 |
| rs559656036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656778 | AATATTTCACTGGAA[C/T]GTATGAGTGTATTAG | 4215 |
| rs559682727 | in-del | -/CTCT | 0.0119091 | 0.0762411 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675682 | TGGGAAACTGTGGGC[-/CTCT]CTCTGAACAGTGGAA | 4215 |
| rs559744845 | snp | G/T | | | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695817 | CAAGCCAACAAACCC[G/T]GCACTCCAAAAAAGC | 4215 |
| rs559768757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641812 | CAGAAGTCAGAAGTC[G/T]CAAGGTTGAGGAATG | 4215 |
| rs559786662 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621318 | ACAATTGTTTTGGAA[A/G]GATATTTGGTGGCAC | 4215 |
| rs559798314 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641367 | CCTGCCTCAGCCTCC[C/T]GAATAGCTGGGATTA | 4215 |
| rs559799091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657385 | TGAATCTTTATGAAT[G/T]GAATTGAATATGTAT | 4215 |
| rs559861455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664120 | GGCGTGGTAGCGGGC[A/G]CCTGTAGTCCCAGCT | 4215 |
| rs560009151 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674955 | GGACCAGCTTCCAGT[C/T]CTAGTACCGATTTGA | 4215 |
| rs560061493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659814 | GGGACAGGCATGAGC[C/T]ACTGTGCCCGGCCGT | 4215 |
| rs560085244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666773 | AGCGAATAGTGGTTT[G/T]CTGAGACAAATAGAA | 4215 |
| rs560086388 | snp | A/G | 4.98542e-05 | 0.00499245 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691722 | CTCCTCTGACTTCTT[A/G]TGGCCTCCAGGGCTC | 4215 |
| rs560122367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665679 | TATGTGGCTTTGACT[C/G]TTGTTTCCTTTTTGA | 4215 |
| rs560123977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627097 | TGGCTTCCTGCTGGA[A/G]CTAAAGAGAGGAGTA | 4215 |
| rs560148353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674415 | CTGTCACCCAGGCTG[A/G]AGTGCAGTGGTGCCA | 4215 |
| rs560150795 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627971 | AATGTGTTGGCATAG[A/T]CTTGGCTCACTGCAA | 4215 |
| rs560227836 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687525 | TCAAAAAGAAAAAAA[A/T]AAAAAGCAAAAAAAA | 4215 |
| rs560301162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682215 | CCAGCTCATTTCAGT[A/G]GTGTTTTAACATACG | 4215 |
| rs560361529 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643522 | GTCTCAATAATAACA[A/T]TAATAATAATAGGGG | 4215 |
| rs560422686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651907 | TTATGGCATCTCAAA[C/G]ATGAACGATGGAAAA | 4215 |
| rs560471088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642627 | CGCGCCACTGCACTC[C/T]AGCCTGGGCAACAGA | 4215 |
| rs560490383 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622390 | GTGAGTGACAGACAG[A/G]GGGGCGAGCTGCGCG | 4215 |
| rs560502488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636665 | AGATCCAGCATGTGT[C/G]TCCCATGTGCCAAGT | 4215 |
| rs560612117 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628410 | TTGTTGCCCAGGCTG[G/T]AGTGCAATGGCACCA | 4215 |
| rs560655467 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636982 | GGTGCCCATGGGCTA[A/C]GGTATCCGGAAGCTG | 4215 |
| rs560675304 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627891 | GCCCGGCCTGTCACT[C/G]TTATTTTCTTCAATC | 4215 |
| rs560746550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664552 | AATTTGTGGGTGGAC[C/T]TTTGTAACTTATTTT | 4215 |
| rs560809736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671590 | ATGCTAAGACATGAC[A/G]CTCAATTCTCTCACA | 4215 |
| rs560828294 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677981 | TACTCATGGGGGACA[A/G]ATGGCCTGGCCAGTT | 4215 |
| rs560843947 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644733 | CTTTAGGCATCTACC[C/T]TTCCTTTCAAACTCA | 4215 |
| rs560900558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681522 | GGGGTTATTCTGGTT[C/T]CTGTTTTGTGTCAAG | 4215 |
| rs560912535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665164 | AAAAAATTAGCTGGG[C/T]GTGGTGGCACATGCC | 4215 |
| rs560939138 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620328 | GGGGTGGATAATGAA[A/G]AAAAGGTTGAGAAAC | 4215 |
| rs560973884 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672118 | TGAAACCCCGTCTCT[A/C]TGAAAAATACAAAAA | 4215 |
| rs561078350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673664 | GCCTATAATCTTAAC[A/C]CTTTGGGAGGCCAAG | 4215 |
| rs561079128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678213 | CACCACTGCAGGGGT[A/G]TAGTAAGGGTTAAAT | 4215 |
| rs561090092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688466 | GGGAGACTGCCTGGA[C/T]GCCCTGCTTGGTTGC | 4215 |
| rs561142724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690094 | TCTGACTTCAGGTCC[A/G]AGTGACTAGGGCACT | 4215 |
| rs561146314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686478 | CAAGAGTGCCAGGGC[C/T]TGCTGTCATAGACTG | 4215 |
| rs561184149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651223 | GCATGGTGGCTTACA[C/T]CTATAATACCAGCAC | 4215 |
| rs561188825 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641749 | AGAGATTGAGGAATC[A/G/T]TCTATTTAGAGGCCC | 4215 |
| rs561215005 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694657 | CCAGCCTTTGTTCCC[C/T]ACTGGAGCAGAAGGG | 4215 |
| rs561256575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629124 | CTAAGAAAGTTGTTA[C/T]TTGTTGTTTTTTTTT | 4215 |
| rs561258321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658740 | ATTTCTTTTCTTTTT[C/T]TTTTTTTTTTTGAGA | 4215 |
| rs561328019 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695659 | CCTGGCCCGCACCCC[A/C]ATCCCCAGTCCCTGT | 4215 |
| rs561385716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636542 | AGTGAGTTATCAATG[A/G]GTGTTAGTTCTCTGT | 4215 |
| rs561446836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643459 | AAGGCTGCAGTGAGC[C/T]GTGATCGTACCACTG | 4215 |
| rs561638138 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674386 | CCCAGGCAACATGGC[A/G]AAACCCCATCTCTCT | 4215 |
| rs561654707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645643 | TAGCTAGAAAGCATC[A/G]GCAGCAAAATTTCTT | 4215 |
| rs561694980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667288 | TATAGTAGTGTGATT[A/C]AATTCCTTTTAAACA | 4215 |
| rs561715323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653363 | AATTGAGTTAGGGGT[A/G]CAAGACAAGAAAGCT | 4215 |
| rs561759089 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652722 | TTTTTCTCTCTGTTT[-/A]CCAGAGCCTTTAAAG | 4215 |
| rs561774987 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628651 | AGGCGTGAGCCCCTG[G/T]GCCCTGCCAATTCTA | 4215 |
| rs561811312 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625285 | TGTAAATAATAGGAA[A/T]TTTTTTTTTTTGCTT | 4215 |
| rs561829122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660702 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC | 4215 |
| rs561875137 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624648 | CAGTTGTCCTCCTGT[C/T]AGTTTTACGTGAAGA | 4215 |
| rs561900703 | in-del | -/GT | 0.0119091 | 0.0762411 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626346 | CAATTAAGTGCAAAA[-/GT]GTGTAAAGATATACA | 4215 |
| rs561932607 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622315 | TCTTGTTATTGGCTG[A/G]TGAGGTGGGTGGGGG | 4215 |
| rs561992510 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621620 | GGTGTGGCCCTGGAG[C/G]TGTGAGACAGGGAAA | 4215 |
| rs562004480 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631215 | TGTTTGAGCCTGGGG[A/G]TGGAGGAGGCTGCAG | 4215 |
| rs562139427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662063 | AGCCAGGATTGCGCC[A/G]TTGCACTCCAGCCTG | 4215 |
| rs562214039 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675709 | AGTGGAACTGCTACT[C/G]TGCTCCTTTGCTTCA | 4215 |
| rs562224777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691966 | TGAACTTTCTGAAAA[C/G]TGGGACCCCAGTTGT | 4215 |
| rs562230142 | snp | A/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688005 | GGACTGTGTGTGCCT[A/T]ATCTGTAGGGGTGTC | 4215 |
| rs562230655 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636974 | TCCAAGCTGGTGCCC[A/G]TGGGCTACGGTATCC | 4215 |
| rs562270668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683592 | AAGGCAGTGGTTGGG[A/G]ATTGCCAAGGTCCTC | 4215 |
| rs562271116 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666220 | GCACAATGGTACTTA[C/T]GATAGCTTTTCCCAA | 4215 |
| rs562286093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683253 | TTTGTACTCTTCTTC[C/T]TTCTATACTCCTGCC | 4215 |
| rs562343818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682531 | ATCAAGGTGTCAGCC[A/T]GGCTGCCTGCCTTTC | 4215 |
| rs562444171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691297 | CCTGGGGGCTGGGGC[C/T]TGCAGGAGGGGGGTC | 4215 |
| rs562515489 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660546 | GTTTTGAATTGTGCT[A/G]TCTCTTTCTTCTCTT | 4215 |
| rs562579311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666572 | TCCTCCTCTGCAGAA[A/G]TAATTTTCTGCTACT | 4215 |
| rs562639870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672593 | GTTATGTTGAAACCA[C/T]GCACCCAGGCGAGAG | 4215 |
| rs562642864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665828 | CTGGCATGGGGACTA[C/T]AGGAGGTTGCTTGGC | 4215 |
| rs562668701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628517 | AGGCATGTGCCACCA[C/T]GCCCAGCTAATTTTG | 4215 |
| rs562672156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631143 | AATACAAAAATTAGC[A/G]GGGCATGGTGGTGTG | 4215 |
| rs562706396 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621428 | AGATTATCTCTGGGG[G/T]GGGATCTTTTCTTTT | 4215 |
| rs562713859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668303 | GACTTTGCCTTACTG[A/G]GTAACTTCTGGAATC | 4215 |
| rs562735491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630016 | ATCCATCTTTGTTCA[A/G]TATCTGAGTTGAAAG | 4215 |
| rs562735880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637516 | AGATCATAGACAGAA[C/T]GTGAAATATTTTGTA | 4215 |
| rs562739332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673540 | CTACGGAAATTCTAC[C/T]TACCTTTGAAGCTCA | 4215 |
| rs562742202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624445 | CCACATGTGTTGACT[A/G]CATCTCATTATCTAA | 4215 |
| rs562778277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675637 | GGCAGCTTAAACCCC[A/G]CTTTTCTCCTTCTGT | 4215 |
| rs562962707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681613 | GAAGGGACTTTGTTT[A/G]CCTGAGGGAGCTGGC | 4215 |
| rs562976875 | in-del | -/AGAT | 0.0279526 | 0.114869 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677848 | ACTCCAAAGAAAGAA[-/AGAT]ACATGGCACTGTGCT | 4215 |
| rs562993886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645323 | AAAAAAGAAACATGA[C/T]AGACCTGATCTCTGC | 4215 |
| rs562999190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675054 | TCTTCAAAGGTTTTT[A/T]TTCCCTCCTTGCTAT | 4215 |
| rs563029432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682283 | TATATTTTAGTTTTG[C/T]TGTTTCTTGATGAAA | 4215 |
| rs563085561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692129 | TTGCAGTTCATGTCT[A/G]ATTCAGTGGTAGCCC | 4215 |
| rs563190624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639129 | AAGTATGATATGACT[A/G]TGCCTCACTGTGTGG | 4215 |
| rs563252910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647360 | TTTTCACATTTTCCA[A/G]CCTGAGTTTTAAAGG | 4215 |
| rs563253582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662007 | ACTCGGGAGGCTGAG[A/G]CAGGAGAATGACATG | 4215 |
| rs563255142 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654839 | TCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACATG | 4215 |
| rs563266490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632528 | AAAATTCAAATTGCC[A/G]TAGTCTGACCTTTTG | 4215 |
| rs563272629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651809 | TTAAGAAAACTGATC[A/G]GGCATATCACTAACT | 4215 |
| rs563280419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630697 | ATGGGATATATATGT[C/G]TTAATTTGACAGATG | 4215 |
| rs563286210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639810 | CAGTGGAAGAGATGA[G/T]TATAAAGCAACCTTC | 4215 |
| rs563476085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646749 | AGAAGTTCTCAGTAG[A/G]AAAAATGTGACTGTA | 4215 |
| rs563511276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649172 | CCAGGTACAGAGGCT[C/T]ACGCCTGTAATCCCA | 4215 |
| rs563709698 | in-del | -/A | 0.279726 | 0.248226 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662245 | ACCCTGTCTCTATTG[-/A]AAAAAAAAAAAAAAA | 4215 |
| rs563721237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656647 | TCTGACATTTGCTAG[A/G]TCCTAAGCAAGGCAT | 4215 |
| rs563785022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656036 | GGAGTTCAAGACCAG[C/T]CTGGACAACATGGTG | 4215 |
| rs563829009 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628881 | TTGACCTTTTCTCAT[G/T]GATGATAATAATAGC | 4215 |
| rs563877895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671112 | CTTGGAGTAGGCTGA[G/T]GAAGTGGAGAGAGGA | 4215 |
| rs563895281 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623535 | CAAAAGAATTTCTCT[A/G]AAATCACTTCCTTTT | 4215 |
| rs563961830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659694 | CACGACACCACGCCC[C/T]GCTAATTTTTGTATT | 4215 |
| rs564000954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633019 | GATCACCTGAAGTCA[A/G]TAGTTTGAGACCAGC | 4215 |
| rs564031875 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654106 | ATTCCTGAGCTCAAG[C/T]GATCTGCCTGCCTCA | 4215 |
| rs564052128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638515 | TCTGCTTTAGTGTTA[C/T]TGTCAGTTATTCCTG | 4215 |
| rs564071286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683495 | TCTGCCCCCTTCACT[G/T]TTTTACTTTGCCTGC | 4215 |
| rs564095724 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661974 | TGGGCGTGGTGGCAG[A/G]TGCCTGTAGTCCCAG | 4215 |
| rs564115293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646578 | TCAGTTGTAAAAGAC[A/T]TTAGCTCCTTTGAGG | 4215 |
| rs564255342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623561 | CTTTTTGTCAGTATT[C/T]ACAATTTCTACTGTG | 4215 |
| rs564304608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655956 | TGTTTTTGGCGAGGC[A/G]CGATGGTTCATGCCT | 4215 |
| rs564511418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663830 | CAAGGAATTCCAGGC[C/T]GCGATGAGCTATGAT | 4215 |
| rs564558639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676411 | CTCACCCCAGACACT[A/C]CATGTAACAGATTGA | 4215 |
| rs564571609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671324 | GCAGTGGTGTGATCT[C/T]GGCTCACTGCAACCT | 4215 |
| rs564581705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632449 | GTGAGCTATGATCAC[A/G]CCACTGCACTCCAGC | 4215 |
| rs564623042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684187 | ATGTAACGTCCTTCA[C/T]TCCCTGCTTGACTTC | 4215 |
| rs564642458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669432 | CACTGAAAATGTTTG[C/T]CCCTTATACCCATCA | 4215 |
| rs564719581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640832 | AGAGTATAGAACTTG[A/G]TTCTGTTCCTAGCTC | 4215 |
| rs564721443 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633142 | CTGAGACAGGAGAAT[C/T]GCTTGAACCTGGAAG | 4215 |
| rs564733733 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623615 | TTAATGTCTTCCGCA[C/T]GTAGCATTTGAGTTG | 4215 |
| rs564763119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624800 | CTTTTTTGTGAGGGG[A/G]AAGTAGATGACCTTG | 4215 |
| rs564786885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627168 | GAGAAGAAAAACTAC[A/C]TGCCACTGGGGAATT | 4215 |
| rs564791421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639043 | AAAGAAAAAAGAAAG[A/G]TATGTCATATTCCCT | 4215 |
| rs564792523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640010 | CGGAGGTCTTTGAGA[A/G]GAGAATTGAAATTTG | 4215 |
| rs564927475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678724 | ACAACTGACTTAATA[C/T]AGAAGAATTAAAGAG | 4215 |
| rs564958504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688270 | AAGGCCAAGGAGGGA[A/G]AGGGCTGTGCAGCCA | 4215 |
| rs565020335 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695484 | GTTCCCCCAGGGGCT[C/T]TATCAGCCCCTGTAC | 4215 |
| rs565051475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648402 | GGAGGGGTATGATTT[A/G]CTATTAGGCATTAAT | 4215 |
| rs565114121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685778 | AATGTAATAATAGCT[C/T]ATAAAATAGCAGCTC | 4215 |
| rs565159894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693494 | TGCAGTGGTGGGCAG[A/G]ACAGCTGGGAGTCCA | 4215 |
| rs565169950 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645119 | TCATTCAACCACTTA[A/G]CAAATATTATTAAGC | 4215 |
| rs565177672 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682159 | CAGATTTTTCTTCAT[C/T]GTGGTCCTCTCATTG | 4215 |
| rs565207683 | snp | G/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678768 | GGTGCAGTGGCTGAC[G/T]CCTGTAATCCCAGCA | 4215 |
| rs565245897 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664319 | AAATTTAATTAAATC[A/C]CCTCAGATGCTTTCA | 4215 |
| rs565270633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635644 | GGTATTTATAGCCTA[A/G]TATAATGAAAGGAGC | 4215 |
| rs565316809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650212 | TTGCCTTTTCTATTA[A/G]ATTGTCTTTTATTGA | 4215 |
| rs565334599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642686 | ATAAATAAAATGTTG[C/T]CCCAGTTTAAGAATG | 4215 |
| rs565352149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669732 | GTTGGGATTACAGGC[A/G]TGAGCCACCACGCCT | 4215 |
| rs565384291 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657612 | ACAAATTTTTGGATT[G/T]TACATTTAGAGAAAA | 4215 |
| rs565397726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642034 | CAAATTATCTTTATC[C/T]GAACTTCCCTTATCT | 4215 |
| rs565415944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676880 | GACTGCTCAGGAACA[A/G]CAGGAAGCCTGTTAA | 4215 |
| rs565479760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675909 | TGCTGGTAAATACGT[A/G]GTTTTATGGTCCAGT | 4215 |
| rs565541448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683659 | CCTGGTAACAGGCCA[C/T]TTGAGATCAATCTGC | 4215 |
| rs565546259 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657354 | CATTAAGTGAAAGAA[C/G]CTAGATGAAAAAGAT | 4215 |
| rs565742259 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625691 | AGCAGCTGTTTTGAT[A/T]GAAATTTGAATCACA | 4215 |
| rs565747757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668917 | TCCGCCTGGGAGAGA[A/G]GGGCTTTCACAGAAA | 4215 |
| rs565783856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638779 | CGGTCAGGAGTGGTG[G/T]CTCATGCCTGTAACC | 4215 |
| rs565803929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624980 | GAATTTCCAGTTTAG[G/T]TAGTTTGCTTTTAGT | 4215 |
| rs565806776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684460 | CAGTTTTACTTTGCA[A/G]TTAATTTGCCTTGAT | 4215 |
| rs565976279 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638077 | AGGGTTGTTGATAAG[A/G]TGGGCTGGCCAGTTT | 4215 |
| rs565985126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633551 | TTTGTTATTACTGTT[C/T]ACAGTTATTTTACCT | 4215 |
| rs566047818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634188 | TCATTTGTATTCAAA[G/T]CCACTTTTCGAAGGA | 4215 |
| rs566055347 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623804 | TAAAAGGGTAAACTT[A/C]AGTGAGAGGATCGTT | 4215 |
| rs566086942 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686796 | CTTCTCATTGTGAAT[A/G]ACCTGGACTTATTTC | 4215 |
| rs566090338 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634380 | GGGAAGCTTTCTTGA[A/G]TTGGAAGGCCCAAAA | 4215 |
| rs566116724 | snp | A/C | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684619 | TGAATTTTCATAATT[A/C]TGATACTTTGTTTCC | 4215 |
| rs566124273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641304 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTTGCT | 4215 |
| rs566137810 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636888 | CAAGCCTTGGGACAA[C/T]GAGACCAATATAGCC | 4215 |
| rs566150269 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694152 | CCAGGGTATGAAGAG[A/T]GTTATTTTCATTCAA | 4215 |
| rs566153526 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665196 | GTAATCCCAGCTACT[C/T]GGGAGGCCGACCAGG | 4215 |
| rs566163398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650610 | GCCTGGCTTGTCTTC[G/T]GTATTTTATGTTATG | 4215 |
| rs566291838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656253 | AAATCTTGTATTATA[A/G]ATTGGGAACTGTGTA | 4215 |
| rs566309770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647935 | CCACTTATCCATGAC[A/G]GGTATTCATTCTGGT | 4215 |
| rs566361140 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653143 | AGCACCTGCTCCAAT[A/G]AGTTCTTTAACTCCT | 4215 |
| rs566486410 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695161 | ATTAGTGCCAGGCAG[C/T]CCTGCCAGCCATGCC | 4215 |
| rs566559392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666112 | CCCTTTGTTGCTTAG[C/T]TTTCTCTGGCGGCTG | 4215 |
| rs566683152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672832 | GACAGAAACCTGTTA[C/T]TTTCATTCACAGATG | 4215 |
| rs566690562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671614 | TCTCACAAGGGTACA[A/G]TGGAGGTTTCCAGAG | 4215 |
| rs566752561 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671345 | ACTGCAACCTCCGCC[C/T]CCCGGGTTCAAACGA | 4215 |
| rs566829980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642893 | TTTCCAAGTAGCTAA[A/G]ACTACAGGCGTGTGC | 4215 |
| rs566849672 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642735 | TGTGTTTTTAACCTC[A/G]TTTTTTTGTTTTGTT | 4215 |
| rs566872675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629194 | GTAGCGCTATCTCAG[C/T]TCACACCAACCTCCG | 4215 |
| rs566909150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680691 | CTGTCATTCACTAAC[A/G]TTAGGATGATAAACC | 4215 |
| rs566927506 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664867 | TCAAGGTGTCCTAAA[A/C]CCTTGAAGCAACCTC | 4215 |
| rs567061141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635279 | TTCATTCCTTACACA[C/T]GTCATGAGTTTCTGT | 4215 |
| rs567062077 | in-del | -/TAAG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628825 | GTTCAGTAATAAAAT[-/TAAG]TATTAGGGTAGATTA | 4215 |
| rs567098438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635840 | ATGAAAGATCAAAAC[C/G]TAATTTAAATGGTGA | 4215 |
| rs567099639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687786 | CAAGGTCAAGAGATC[A/G]AGACCATCTTGGCCA | 4215 |
| rs567139392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688689 | TCAGTAGCTCTCCTT[A/G]GGCTTGCTGCTTTGA | 4215 |
| rs567175228 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626477 | TATATATTGATTCTT[A/T]TGAGGAATAAATGGC | 4215 |
| rs567215253 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641826 | CGCAAGGTTGAGGAA[C/T]GGTCATGTGTTTGGG | 4215 |
| rs567220792 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695734 | CGTCCCAGGTTCAGG[A/G]TCTTACAGAGCTCCA | 4215 |
| rs567287746 | snp | G/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679655 | AATTTTTAAAATATT[G/T]TTTGTAGAGATGGGG | 4215 |
| rs567398333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679728 | AGCATTTCTCCTGCC[C/T]CTCGAAGTGTCGGGA | 4215 |
| rs567407561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671334 | GATCTCGGCTCACTG[C/T]AACCTCCGCCTCCCG | 4215 |
| rs567430941 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668194 | GATCCTGAGCTGAGC[C/T]TGAGAGATCTAAGCA | 4215 |
| rs567436040 | in-del | -/GTG | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638843 | CCTGGCCTGGCCAAC[-/GTG]GTGAAACCCTGTCTG | 4215 |
| rs567445752 | in-del | -/ATT | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683206 | TGTAACTTTTCTTTC[-/ATT]ATTCAAACTATGTAG | 4215 |
| rs567464090 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679246 | AGAGCAAGCCTCCCC[A/G]CCATTCTTTTTTTCC | 4215 |
| rs567520700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687717 | GTCTGGGGCTGGGCG[C/T]GGTGGCTCATGCCTG | 4215 |
| rs567582686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687155 | CGGATCACCTGAGGT[C/T]AGGAGTTTGAGACCA | 4215 |
| rs567589055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677011 | GTGGAATCCATCTTA[C/T]GCCTACCCCATATAT | 4215 |
| rs567628552 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678698 | ACAACCACATGAACC[-/AT]ATGTTCTGAACAACT | 4215 |
| rs567631645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650355 | TGCCCAGGCTGGAGT[A/G]CAGTGGTGTGATCTC | 4215 |
| rs567634187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671936 | AGGATGGCTTGATTC[C/T]AGGAGTTTGAGCTTA | 4215 |
| rs567656031 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620781 | AGGCCGAGGCTGGCG[C/G]ATCACCTGAGGTCTG | 4215 |
| rs567681102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647328 | GAGAAGTTAAATTGT[C/T]ACTTCACTGTTGCTA | 4215 |
| rs567715374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628609 | AGGTGATCCACCTGC[C/T]TTAGCCTCCCAAAGT | 4215 |
| rs567737737 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650587 | GGATTACAGGCATGA[A/G]CCATCTTGCCTGGCT | 4215 |
| rs567782465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628105 | GTGATGAGGTTTCAC[C/T]ATGTTGACCAGGCTG | 4215 |
| rs567834162 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635191 | TGACTTTATGCACTA[C/T]GTAAGGGACTGTTGA | 4215 |
| rs567876706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641404 | CCCGCCACCACACCC[A/G]GCTAATTTTTGTATG | 4215 |
| rs567889306 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694424 | GACCCTGCCTCTCCC[A/G]GGCAGGGGCCCGCGA | 4215 |
| rs567913878 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694908 | TCCCTTGTAGCTCCT[C/T]CCCTGGAGGGGGAAT | 4215 |
| rs567933206 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638219 | AATAAAATTTTAATT[-/TTTG]TTGTATTTTTTTTTC | 4215 |
| rs567947583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637073 | ACCAAGTTTGAGAGC[A/G]TGTGTAGAGTGTCGA | 4215 |
| rs567965559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690502 | GCCTGAGATGCTGTA[G/T]GTTGCTTCCTCTGTC | 4215 |
| rs568014547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644964 | TCTGTAATATCTCTC[C/T]CCTTTCCCTGTCATT | 4215 |
| rs568068248 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681161 | CATAAGCCAGGAAGT[A/G]TGGGAGTGGGTAGGA | 4215 |
| rs568079468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654355 | CTTCTTTGACTAAGC[A/G]TATGTTTTCAACGGT | 4215 |
| rs568112838 | snp | C/T | 2.72224e-05 | 0.00368923 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689765 | CTGGCTAGGAGGAGA[C/T]TGCCCAGGTGGTCTC | 4215 |
| rs568134392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642994 | AACTCCTGGGCTCAA[G/T]CAATCCTCAAACCTC | 4215 |
| rs568152264 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696044 | TGCCGTCACTTTCTC[A/G]TCATTCCATGGGGTG | 4215 |
| rs568157483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643984 | TCTTCCTTTACAAGC[A/G]ATATGACCTGACCTT | 4215 |
| rs568175731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696734 | GGTCATCTGCTACTG[A/T]TGCTTAACCGAACCA | 4215 |
| rs568184154 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661164 | TGATTCTCCTGCCTC[A/G]GCCTCCTGAGTAGCT | 4215 |
| rs568202598 | in-del | -/T | 0.0279526 | 0.114869 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659036 | CACTGTGCCCGGCCA[-/T]TTTTTTAATTTTTTT | 4215 |
| rs568288336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659971 | CTCTAAAGTTTTTCA[A/G]AGGGCCCTCTCCATT | 4215 |
| rs568296450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651439 | TATCATTGCCACTGC[A/T]CTCCAGCCTAGGTGA | 4215 |
| rs568352233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659146 | CAAAGTGCTGGGATT[A/T]CAAGTGTGAGCCACT | 4215 |
| rs568373016 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622966 | TCCGCGGGGCGGCCC[A/G]GCCGGCAGAGCCCGC | 4215 |
| rs568453312 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661661 | TGACAAAAATAAGCT[G/T]CTAATCTTCTCACCT | 4215 |
| rs568640776 | snp | A/G | | | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666980 | TGTCCAGACAGGTGC[A/G]GATCAAGGCTTCCCA | 4215 |
| rs568655432 | snp | C/T | 1.68695e-05 | 0.00290422 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667084 | TTCAACCCTTTTTTC[C/T]CCCCCTCTATTTTAT | 4215 |
| rs568689155 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675142 | AAAATGGGAATTTTG[A/T]AAGTTGAAACATAGA | 4215 |
| rs568813447 | snp | C/T | 0.000216439 | 0.0104006 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681760 | AGCCTCCTTTATGTG[C/T]TCTAGGCTCCCAGAA | 4215 |
| rs568813546 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674005 | CAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC | 4215 |
| rs568874206 | snp | C/T | 3.29641e-05 | 0.00405968 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688850 | CCCCCGGCGCTACCA[C/T]GTGTCTGTGCACCAC | 4215 |
| rs568875104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642944 | TGTATTTTTTGTAGA[A/G]ATGGCGTTTTGCCAT | 4215 |
| rs568878361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696583 | CCTCACAACCTGAAC[A/G]TCACCAGTGGCTGAG | 4215 |
| rs568924182 | snp | A/T | 0.369958 | 0.21934 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650695 | GAGAGAGAGAGAGAG[A/T]GTTTTTTTTTTTTTT | 4215 |
| rs568935735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651368 | GTCCCAGCTACTTGG[A/G]AAGCTGAGGCAGGAG | 4215 |
| rs568957337 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638005 | CAGTGATTGAGCAGA[C/T]TGTCTTTTGCTTTCA | 4215 |
| rs569010486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660299 | TCAACCTCCCAGACT[C/G]AAGTTATCTTCCTCC | 4215 |
| rs569045006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659120 | CAAATGATCCACCCA[C/T]TTTAGCCTTGCAAAG | 4215 |
| rs569108679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665285 | CTTCTTCTGCCTCAG[C/T]CTCCTGAGTAGCTGG | 4215 |
| rs569108789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658167 | ATACTTTATGATAAA[A/G]AATAAAATTCTTGTG | 4215 |
| rs569163626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629268 | GCTGGGATTACAGGC[A/G]CACACCACCACGCGC | 4215 |
| rs569170645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664758 | TACACAGTTCATACC[A/T]ATGGGCTCTCCTGTC | 4215 |
| rs569197239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652939 | GGGCTAGGGCTTATA[C/G]TGTCTCCTTTACATT | 4215 |
| rs569221846 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628792 | TATTCAGTAAATTGT[C/G/T]GTTAATGATTTATAA | 4215 |
| rs569279279 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622694 | GCCGCCCGGGCCCCC[A/G]GCATGCAGCCCCGGC | 4215 |
| rs569312173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674540 | TTTTTGTAGAGATGA[A/G]TTCTCACTATGTTGC | 4215 |
| rs569422395 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621866 | GGAAGGCCTGAGGGC[C/T]CCCTGCAGCCGCCTA | 4215 |
| rs569454532 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682742 | TCAAAGCCAGCAGGA[A/G]AATCTTTTGCTCCAA | 4215 |
| rs569457392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673924 | AAAAATAAAAAATAA[A/T]TAAAAATTATCCAGG | 4215 |
| rs569503123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668780 | GGAAAATGGGCAACA[C/T]GGCCTCTTAGCATAC | 4215 |
| rs569538128 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624910 | TGTATACACAGATAC[A/G]TTCACACACAGTCTC | 4215 |
| rs569566466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675816 | CTGTGACCCCTGCCT[A/G]TGCAGCCTTCTGAGA | 4215 |
| rs569649241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667953 | TCAGGCCTGTGCATT[A/T]TTACTTGTTAACCCA | 4215 |
| rs569688372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624044 | GAGAAGGGTTTGTTC[A/G]TTTGCTGGGCTTACT | 4215 |
| rs569691466 | snp | A/G | 4.94996e-05 | 0.00497467 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632828 | CCCTGGCAGAGCTAA[A/G]TGAGATTTGTTGGGG | 4215 |
| rs569697642 | snp | A/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671427 | CACCCAGCTAAATTT[A/T]GTATTTTTAGTAGAG | 4215 |
| rs569710181 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675446 | CATCAGCTTCCTGAT[A/T]AGGGTTCTGCTATGA | 4215 |
| rs569790980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645951 | CCTAATGTTGCTAAC[A/G]AACTGCCCAAGGCTT | 4215 |
| rs569842922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637872 | ACCCTCCAGATGTTC[A/G]TGAGTGGGTGCTTCA | 4215 |
| rs569853875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653536 | GAATTCCTGATGTTT[C/G]TTTATTCTAAAGCCA | 4215 |
| rs569933939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645126 | ACCACTTAACAAATA[C/T]TATTAAGCACAAATA | 4215 |
| rs570052641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647788 | TTTCGTGTATTTCAC[A/G]TCAGGATTTTGTAGA | 4215 |
| rs570071922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684690 | AGAAACAAGATCTCA[C/G]TATGTTGCCCAGGCT | 4215 |
| rs570205558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647077 | GTAGTTCTCTACAGT[C/T]GGTACCTTTCAGCCT | 4215 |
| rs570222627 | in-del | -/A | 0.0283406 | 0.115616 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656440 | AACCCAGTCTCTACT[-/A]AAAAAAAAAAAAAAA | 4215 |
| rs570227516 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692547 | CAGGCTGCAGTGTGT[A/G]CAAGGGTATTATTGG | 4215 |
| rs570229520 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653474 | TTAGTAAAGACTTTT[C/G]TGAATCATTTAGTAC | 4215 |
| rs570268245 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688513 | AGTCTGTTTTTTCTT[C/T]TTGTTTTCTCCAGCC | 4215 |
| rs570287624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654593 | CCTAGGCGTGGAATT[G/T]CTGGGTCATAAGATA | 4215 |
| rs570326873 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624280 | AATCTTCGAATTGAT[G/T]TATGAGCCTGTATTG | 4215 |
| rs570334927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631381 | TTTCTTTCCACAGGG[A/T]ATTAGAATATTTCCA | 4215 |
| rs570352128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662214 | AGTTTGAGACCAGCC[C/T]GAGCAACATGGCGAA | 4215 |
| rs570378420 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682690 | AGGCCACCTGCAGTT[C/T]CTTGCCATGGGGCCC | 4215 |
| rs570390488 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656272 | GGGAACTGTGTAAGT[C/T]AATTGGACTTTTGCT | 4215 |
| rs570494429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638822 | GAGGCCGAGGCAGGC[A/G]GATCACCTGGCCTGG | 4215 |
| rs570508115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637718 | TCTGATGATCTTTGC[A/G]AATTTCTGAAGCTAG | 4215 |
| rs570553676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646934 | TTGATATACTACCCC[A/C]TGCCACCCTCAGCTT | 4215 |
| rs570557001 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656497 | GTAATCCCGGCTACT[C/G]TGGAGGCTAAGGCAG | 4215 |
| rs570569452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637098 | TGTCGATGTTGCAGC[A/T]TTCAACAAGGTCTGA | 4215 |
| rs570575926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690593 | GTCTGAAGAGCACCA[A/T]GCACCTGGAGGGGAG | 4215 |
| rs570630222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645021 | TGCCCTTTTGCAATA[G/T]CTCTTCCTCTTTAAT | 4215 |
| rs570675725 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676823 | GGAGACCAGGTGTGG[A/G]GCCTCTGCTAACACT | 4215 |
| rs570805920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647654 | CATTCTCTTTTTACG[C/G]AGCTGTTTTCAGGAG | 4215 |
| rs570864190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654367 | AGCGTATGTTTTCAA[C/T]GGTCATCTGTGCATG | 4215 |
| rs570927256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662124 | ATAATAATAACATTG[A/G]GCTGGGCATGGTGGC | 4215 |
| rs570943535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663371 | GCTGAGCGTGGTGGC[A/G]CATGCCCGCAATCCC | 4215 |
| rs570995497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653771 | TAATTATAGTTTTAT[C/T]GAGATTAAAAAATTT | 4215 |
| rs571004724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670472 | CCTCTAGTCCCAGCT[A/G]CTCAGGGGGCTGAGG | 4215 |
| rs571011893 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624527 | TTTATAAGTGTGTGA[A/G]TATATGGAGACCAAT | 4215 |
| rs571059356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661841 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 4215 |
| rs571070301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669883 | GAGTTGGGTGGATTG[C/T]TTGAGCCTCAGGAGT | 4215 |
| rs571090872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668632 | AGAGCCTATGATATG[C/T]GCATGGAGGCAGGGG | 4215 |
| rs571122064 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660015 | GGTGGAAGAGCAGGA[C/T]GAGCAGTATACCAGT | 4215 |
| rs571144203 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628470 | GCTTGAAGCAGTTCT[C/T]CTGCCTCAGCCTCCC | 4215 |
| rs571155830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667815 | TATTCTCAATCTGTG[G/T]TTGGTTGAATCCACA | 4215 |
| rs571263413 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651054 | TCTTATATTCTTTTC[G/T]TCAGTTATCTCTGAT | 4215 |
| rs571344645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625905 | GGTGAAACCCTGTCT[C/G]TACTAAAAACACACA | 4215 |
| rs571376814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677557 | TGTGAGGTCTGGGTC[A/G]CTGGAAAGTGGAGTA | 4215 |
| rs571377687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676978 | AGCTTCTCAAGTACA[G/T]GAAGGCACAGTAGAA | 4215 |
| rs571452738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687053 | CAAGAACATAGACTT[C/T]GGGTTCATAGACCTG | 4215 |
| rs571471382 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673095 | CTACTCAGTTCACAC[C/T]GGAACATTTGCATTG | 4215 |
| rs571533650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632117 | GGCACTGGACCAACT[A/G]CCCTGTTTGAGCGTG | 4215 |
| rs571561880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683879 | AAATTATGTCAGTCC[A/G]GTCGCAGTGGCTCAT | 4215 |
| rs571595360 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642354 | GATTCCTTCATTAGT[A/T]TATCTAAATATAATG | 4215 |
| rs571612955 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692949 | AGGATTAGGTTAAGG[A/G]TTTTGAGATGGATGG | 4215 |
| rs571649369 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663204 | ATATATGAACAGTGT[-/A]AAAGTTTACAATGCT | 4215 |
| rs571721822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634870 | CATGCTGCAACAGCA[A/G]AATTCACTTCCCAGA | 4215 |
| rs571849121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641365 | CTCCTGCCTCAGCCT[C/T]CCGAATAGCTGGGAT | 4215 |
| rs571849375 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635643 | AGGTATTTATAGCCT[A/G]GTATAATGAAAGGAG | 4215 |
| rs571850578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648695 | TGGCCGGCGTCTGTA[A/G]TCCCAGCTACTCGGG | 4215 |
| rs571852033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649385 | GAGCTTGCAGTGAGC[C/T]GAGATCGTGCCACTT | 4215 |
| rs571904786 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684170 | AACAAAATGCTAGCA[C/T]AATGTAACGTCCTTC | 4215 |
| rs571917215 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656821 | CTGCTGTAAAAAACT[A/G]CCCAAGACTGGGTAA | 4215 |
| rs571992374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674795 | TCCAGGTAGAGGGTT[C/T]ATAATACTTTTGCAA | 4215 |
| rs572026447 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654774 | AGGTGCAGTGACTCA[C/T]GCCTGTTAATCCCAG | 4215 |
| rs572026793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646441 | GCAGGATTCTCCTGT[C/G]ATATGGTGCCATTAC | 4215 |
| rs572055816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682050 | GCCCAAATATGGATT[G/T]TCCCTTTTTAAGGGC | 4215 |
| rs572087184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668065 | ATCTGGTCTTATCAA[A/C]CATCGTGTTGAGCCT | 4215 |
| rs572088726 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653962 | GCCTTGACCTCCTGC[A/G]CTCAAGCGATTCCCC | 4215 |
| rs572122854 | in-del | -/AA | 0.00159617 | 0.0282053 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696256 | GAGGGCTTGCAGTGC[-/AA]AGCCAGGCCAGTGTT | 4215 |
| rs572216075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625315 | TTGATACTATGTGGC[C/T]ATAAAAAATTGGGAT | 4215 |
| rs572225541 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667332 | GATTGCCTCAGACAT[A/C]TGCTTGAAGACTTCC | 4215 |
| rs572251785 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624109 | CTCTTCTGAGGGAAG[G/T]TCTGCTGTGAGAGTG | 4215 |
| rs572256808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630967 | GGGCACCAGAGCAGA[C/T]TTCGTCTAGGAAGAG | 4215 |
| rs572305886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662988 | CCCCAGAAGAGGGTT[C/T]TTAGAATTATTGTAG | 4215 |
| rs572422387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656664 | CCTAAGCAAGGCATA[C/T]GTTTGCATCTTATGA | 4215 |
| rs572428504 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670966 | AGAGGAGTGGGTGAT[A/G]TTACATATTCGTATT | 4215 |
| rs572494227 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63670114 | TCTCAAAAAAAAAAA[A/T]AGTAATTACCAAAGT | 4215 |
| rs572537846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641597 | AACCTAAGTTCGAGG[A/T]TACACAGCTAGGAAG | 4215 |
| rs572549321 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684925 | AGGGATTCCAAAGGC[C/T]TTTTGTTGCTGCATT | 4215 |
| rs572552945 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644151 | CAATAAACGTTAGCT[A/G]TTATCATTATTATTA | 4215 |
| rs572575212 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648080 | GAAATGTTAATGACA[C/T]ACTGATGGGGGTGGT | 4215 |
| rs572583285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638982 | AGTGAGCCGAGATCA[C/T]TGCACTCCAGCCTGG | 4215 |
| rs572617293 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676323 | ACCTGTAAAACCAGG[G/T]GAGAGTTCAGTGCAG | 4215 |
| rs572669185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648947 | GGAAGGAATTACCTT[C/T]TTGAGATGTTAGGCT | 4215 |
| rs572735264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692059 | CATGTGGGCCTTGGA[A/G]ATGGTCATTTTGTGC | 4215 |
| rs572759230 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630637 | CAGCCAGGTTCCCTT[A/C]TTTAAAGAAGCTATA | 4215 |
| rs572768154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634577 | AGGCAGAAGCCTAAA[A/G]AGGATTGACTGTTAG | 4215 |
| rs572772470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647183 | TTGTCAGAGGCAACC[C/T]GGTGGAAGCATTGTG | 4215 |
| rs572792618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633899 | ACCAATTCTTCAGAA[A/T]TGGTTCCTAGAGATA | 4215 |
| rs572819446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686196 | CCAAGAACACTTTTG[A/G]TCACGTCTGTCTGGG | 4215 |
| rs572828605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628464 | CTCCCAGCTTGAAGC[A/G]GTTCTCCTGCCTCAG | 4215 |
| rs572893114 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691576 | CTTGGGGTACTCTCT[C/T]TTCCAAACTGCCTGA | 4215 |
| rs572923078 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662193 | GGCAGATTACTTGAG[C/T]CTAGGAGTTTGAGAC | 4215 |
| rs573026019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656534 | CACTTGAACCCAGGA[C/G]GTGGACATTGCAGCA | 4215 |
| rs573040566 | in-del | -/AA | 0.378962 | 0.21417 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664247 | GCGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 4215 |
| rs573087579 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663495 | CGATGAGCGAAACTC[C/T]GTCTCAAAAAAAAAA | 4215 |
| rs573119382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672048 | ATCACTTTGGGAGGC[C/T]GAGATGGGTGGATCA | 4215 |
| rs573154038 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625306 | TTTTTTGCTTTGATA[-/C]TATGTGGCTATAAAA | 4215 |
| rs573240796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642654 | CAGAGTGAGACTCTG[C/T]CTCAAAAAATAAAAA | 4215 |
| rs573245506 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678593 | GCCAGAGAGACATCC[C/T]TGGAGGGAGGCTGGG | 4215 |
| rs573248763 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636816 | GCTGAGGTGGTATGT[A/G]GAGAAGAAGGCCAAG | 4215 |
| rs573291055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685422 | CTTTCATGTTTTGAC[A/G]AAAAGGCCCATTTGC | 4215 |
| rs573322219 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640142 | ACACTGAGCCAGGCA[C/T]GGTGACATGCGCCTG | 4215 |
| rs573377837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664172 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 4215 |
| rs573453859 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655792 | TCCCCAGCCTACTTG[G/T]TTTTTTTTATTTAAC | 4215 |
| rs573515428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662951 | AAGTGCTGGGATTAC[A/C]GTTGTGAGCCACCAC | 4215 |
| rs573516974 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655012 | CATTTGAGACAGAGT[C/T]GAGACTCTGTCTCAA | 4215 |
| rs573555686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640437 | TACGTTGATTTTTGC[A/G]GGTCCATAATCTGTT | 4215 |
| rs573570273 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693875 | CCCAGGCAAGGCTGT[A/G]GACCATGGAGTGGCA | 4215 |
| rs573575643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662409 | GACAGAGTAAGACCC[C/T]GTCTCGAATAATAGT | 4215 |
| rs573618673 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648764 | AAGTTGCAGTGAGCC[A/G]AGTTCGAGCCACTGC | 4215 |
| rs573652685 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648275 | AATGCAGAAGAATTT[A/C]TCTCTGATCATGATC | 4215 |
| rs573654180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633041 | GAGACCAGCCTGGCC[A/G]ACATGGTGAAACCCT | 4215 |
| rs573700514 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676080 | GTTCCTCTGATAGCC[A/G]CTGGTTTGGGGAGAC | 4215 |
| rs573756497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665104 | GGTCAGGAGTTCAAG[A/T]CCAGCCTGACCAACA | 4215 |
| rs573890511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669170 | ATTTCTAACTGGAAT[A/G]ATCTGGAAAATGCAT | 4215 |
| rs573963337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677893 | GCCAGGAAGTCCCCA[C/T]GTTAGCCTCCCTCCC | 4215 |
| rs574036816 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674111 | GACTTGTCCCTGCTA[C/T]ATTCTGACTCCTGTA | 4215 |
| rs574099698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657238 | ACTGTTTGCAACTTG[A/G]TATTTTGAAGTAAAT | 4215 |
| rs574121188 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671414 | GCATGCGCCACCACA[C/T]CCAGCTAAATTTTGT | 4215 |
| rs574207343 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628437 | ACCATCTTGGCTCAC[C/T]GCAACCTCCGCCTCC | 4215 |
| rs574270238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627535 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 4215 |
| rs574333555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626949 | TAAACAGACACCATA[C/T]GGGATAACAATGTTT | 4215 |
| rs574349539 | snp | A/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621773 | CTCGTTACACGCCCT[A/G]TGCTGGGCACGGGGA | 4215 |
| rs574396190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633721 | GGGTACTTTGTTCTG[C/T]AGAGAGGAGTGAATG | 4215 |
| rs574416951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672124 | CCCGTCTCTATGAAA[A/G]ATACAAAAATTAGTT | 4215 |
| rs574430034 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649670 | GCCTTGGCCTTCCAG[A/G]GTTCTGGGATTATAG | 4215 |
| rs574459734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635967 | AAGGTTGTTTATTCA[A/G]GGGTGGAATGGGGCT | 4215 |
| rs574474036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688998 | TCCTGAGGATTTGTG[A/G]CCCAGACTTGAGGCA | 4215 |
| rs574500843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681549 | CAAGGTTTTTTTGGT[C/T]GGATATGCCGTAGTG | 4215 |
| rs574525455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645173 | TTGCCTGGCACTGGG[A/G]ATATAGAAACATGAT | 4215 |
| rs574548900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635583 | CAGCAAATGCATTTC[C/T]AGGAAAGATAGGGTA | 4215 |
| rs574588796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653016 | AAGCAGAGGGTTTAG[C/T]AGGGGCTAGGGAGGT | 4215 |
| rs574588805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644662 | TAGAACCACTCTTGT[A/C]ATTCATTGAACTGGA | 4215 |
| rs574590386 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683655 | TGCTCCTGGTAACAG[A/G]CCATTTGAGATCAAT | 4215 |
| rs574610300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642603 | ACAGAGGCTGCAGTG[A/C]GCCGAGATCGCGCCA | 4215 |
| rs574613679 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679592 | GGCTCAAGCAGTCCT[C/T]CTGTCTCAGTCTTCC | 4215 |
| rs574679615 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694681 | AGAAGGGGAGATGGA[C/T]GACACGGTCGGGGCA | 4215 |
| rs574711996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637340 | GTTTACACAGCTTTT[A/G]CACAAAGGTATTGAG | 4215 |
| rs574750979 | snp | A/C | 0.000422149 | 0.0145223 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690985 | GTCCCCCTTTTCTCC[A/C]ACTGCAGTTCCCAAG | 4215 |
| rs574772748 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659774 | CTGACCTTGTGATCC[G/T]CCCGCCTTGGCCTCC | 4215 |
| rs574812865 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621940 | GCCCGCGCGCCCGCC[A/G]AGCCTTCGGTGACTG | 4215 |
| rs574855177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629871 | CCTGGAAACAGAATT[G/T]GTCAACCTGATAAAC | 4215 |
| rs574899003 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661878 | GGAGGCCGAGGCAGG[C/T]GGATCACAAGGTCAG | 4215 |
| rs574932179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635463 | TCCTCTTAATGAAGT[C/T]AAGGTTATAGAATGG | 4215 |
| rs574951412 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660389 | TTTTTTTTTTTTAAT[G/T]GTTTGTAGAGACAGG | 4215 |
| rs574981383 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663175 | AAAATTTTCAAGGAG[C/T]TGGAGTCACTTTCAT | 4215 |
| rs574995846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634653 | ACTTCAATGTTGTCA[A/G]ACTTATGTTGCACGA | 4215 |
| rs575077101 | snp | A/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694674 | CTGGAGCAGAAGGGG[A/T]GATGGACGACACGGT | 4215 |
| rs575120291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665580 | CCTGCATTCAGGCAG[A/G]TGGCAGGGTGCTCAT | 4215 |
| rs575198273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679520 | CAGGGTCGCACTCTA[A/T]CACCTATGCTGGAGT | 4215 |
| rs575227052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689492 | GGTTTGTACGTTCCG[C/T]CTCGTAGCCTGGGGT | 4215 |
| rs575248432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642441 | AAGGCGGGTGGATCA[C/T]TTGAGGTCAAGAGTT | 4215 |
| rs575384377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659682 | GGATTACAGGTGCAC[A/G]ACACCACGCCCCGCT | 4215 |
| rs575422243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649744 | TCAATTTAAATTTAA[A/C]TAGTCATATGTGGCT | 4215 |
| rs575429512 | snp | A/G | 8.24165e-05 | 0.00641883 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690352 | CTATGACGTGGACAC[A/G]GGACGTGAACTTGCT | 4215 |
| rs575439731 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695258 | GTAGTTTCTATCGCT[C/G]TTTTTAGCCTTTTCA | 4215 |
| rs575503847 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694555 | TGGAGACTGTGTGTG[C/T]CCTCTGGGCTCTGAG | 4215 |
| rs575575913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652385 | ATGCTCAGAGGGTGA[A/C]AGGTAACGGTAGAGA | 4215 |
| rs575648684 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696308 | GGGATCATTTATATC[A/G]GAGGGGTCCTGTGGC | 4215 |
| rs575673672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636471 | GTGTGGCTGGGTCCT[A/G]TGGATAGTTTTGCAG | 4215 |
| rs575679738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665408 | CTGACCTCATGATCC[A/G]CCCGCCTCAGCCTCC | 4215 |
| rs575833643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681997 | GCAGAACTGAGGGAC[A/G]TGAACCCCATTTGAA | 4215 |
| rs575850606 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668372 | TCTGTATATGAATTT[C/T]AGATTTCTGTAGATA | 4215 |
| rs575895577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681339 | GTCCCCACCCTCAAA[A/G]TACTGCTTGGACCCA | 4215 |
| rs575932322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672111 | AACATGGTGAAACCC[C/T]GTCTCTATGAAAAAT | 4215 |
| rs575961666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690030 | TGCATTTGATCAATG[C/G]AGAAGAGCATTTAAC | 4215 |
| rs576006345 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625202 | TGACAACTTGGGTTA[A/G]TAAAAACATGTCAGA | 4215 |
| rs576030933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667223 | GAGAGGAAGGGCAAA[G/T]AAATAACTGGGATGG | 4215 |
| rs576058248 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661913 | TGGAGACCATCCTGG[C/G]TAACACGTGAAACCC | 4215 |
| rs576067318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632257 | AGCACTTTGGGAGGC[C/T]GAGGCAGGAGGATCA | 4215 |
| rs576069325 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643789 | GTGTGGGAAGCTGGA[A/G]ACCACACATCAGAGC | 4215 |
| rs576073704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623441 | TTTTTGAAAAATCCC[A/G]TTGCAGGGGTTTAAT | 4215 |
| rs576119957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661294 | TCAAGTGATCCGCAC[A/G]CCTCAGCTTCTCAAA | 4215 |
| rs576127418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666577 | CTCTGCAGAAATAAT[C/T]TTCTGCTACTCTTCC | 4215 |
| rs576245586 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684979 | TTATTATATTTAGAT[A/G]TCTATTACCTCTGCA | 4215 |
| rs576325270 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656254 | AATCTTGTATTATAA[A/G]TTGGGAACTGTGTAA | 4215 |
| rs576344513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629681 | TTGAAGAACCTGTCT[A/T]CCTCTAGGAATGTAT | 4215 |
| rs576360327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676100 | TTTGGGGAGACTTCC[C/T]TTTCCTGCTCCAGCC | 4215 |
| rs576407364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636887 | TCAAGCCTTGGGACA[A/G]TGAGACCAATATAGC | 4215 |
| rs576493060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638917 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGTG | 4215 |
| rs576533160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638242 | ATTTTTTTTTCCTTT[C/T]ATTCACTTACTCTCT | 4215 |
| rs576574136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684014 | AAAAAAATTTAATTA[A/G]CTGGGCATAGTGGCA | 4215 |
| rs576597047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646342 | GGTCTGACATTTTAT[C/T]AGGAAGTGAGGACTC | 4215 |
| rs576635821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683060 | TTTCAATAAACTTGC[C/T]TTGATGTAAAAGAAA | 4215 |
| rs576635956 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692522 | GGCAGGAGGGAGTGT[G/T]CCCAGGGCCCAGGCT | 4215 |
| rs576654589 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623763 | CACAAGTTTTGCAAA[A/C]TATTTGGTATTGCCC | 4215 |
| rs576698242 | snp | C/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621145 | AAGATTATTCTGGAG[C/G]CTGACATATTACACT | 4215 |
| rs576735136 | snp | A/G | 2.59346e-05 | 0.00360092 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689496 | TGTACGTTCCGCCTC[A/G]TAGCCTGGGGTGTGA | 4215 |
| rs576742520 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646886 | ATAAATGTGCCTTTC[A/G]GTGTTTTTTCCACTC | 4215 |
| rs576798108 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653870 | CTAATTCCAGAACAT[C/T]TTCTTTTTTTTTCTG | 4215 |
| rs576866693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667145 | TTGTTAATTAAATAA[A/T]CATCAAATATTTATT | 4215 |
| rs576869891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638132 | CAAGCCTGGCATTAT[A/G]TTTTGTAAGAAGATT | 4215 |
| rs576914458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681220 | CAGACCATCACGAAG[A/G]CCTTTTTACCTGATA | 4215 |
| rs576927801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646212 | GGATTGGGCATAAAG[A/G]GAGGAAAGTTTCACC | 4215 |
| rs576990600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645269 | TATTGTGCTACTGCA[C/T]TCCAACCTGGGTGAC | 4215 |
| rs577003499 | snp | C/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621617 | GAGGGTGTGGCCCTG[C/G]AGGTGTGAGACAGGG | 4215 |
| rs577037098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689384 | AGTCAGGTGGGAGTG[C/T]GGACGGGATGGGCTG | 4215 |
| rs577044859 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653935 | GCAGTGGTGCAAACA[C/T]GGCTCACTGCAGCCT | 4215 |
| rs577062942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673219 | ACCCACTGATTCTAG[C/T]GCTGCTCCCTTGAGC | 4215 |
| rs577210644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692678 | TTAAGGAAGCAGGAT[C/G]CACTCTGAAGGCCTG | 4215 |
| rs577376542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662325 | GTGGCTGAGGTGGGA[G/T]AATCACCTGAGGCCG | 4215 |
| rs577384322 | snp | A/G | 3.29663e-05 | 0.00405981 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691788 | CAGAGAGCGTGACCC[A/G]AAAGTACACGCGGCA | 4215 |
| rs577437306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661976 | GGCGTGGTGGCAGGT[A/G]CCTGTAGTCCCAGCT | 4215 |
| rs577439328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669014 | GCATAGTAAGGAGCA[C/T]CTGCCAGGCATGATC | 4215 |
| rs577465016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661243 | GTAGAGATGGGGTTT[C/T]GCACTGTTGGCGAGG | 4215 |
| rs577652671 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650547 | ACCTCAGGTGATCCA[A/C]CCACCGCAGCCTCCC | 4215 |
| rs577874340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624383 | TACTTAAGGGTATGT[A/G]GACCATCCACTTCCT | 4215 |
| rs577910464 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647630 | CTTATCAAGGTTTTG[-/A]AAATGGTGCATTCTC | 4215 |
| rs577918830 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635805 | TCTGCCAGAAAGTCC[A/G]TGCTTAGGAAGAGAG | 4215 |
| rs577947447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693133 | GAAACAGGTTCTCCC[C/T]TCAGAGCCTCTGACA | 4215 |
| rs578043303 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664039 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 4215 |
| rs578061528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626827 | GAGCTGGGTAGAACA[C/T]TGTCAAGATGAAGAA | 4215 |
| rs578084138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677866 | TACATGGCACTGTGC[C/T]TCCCCTGTGCTGCCA | 4215 |
| rs578087793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663595 | AAGAGCATGGATAAT[A/G]AAGACACGGATTTAT | 4215 |
| rs578101019 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676749 | TAATCAGGAAGCCAC[C/T]GGTCCAGAAGTCCAG | 4215 |
| rs578107707 | in-del | -/TTTA | 0.00398564 | 0.0444627 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650299 | TTTTGCAATCAGAAG[-/TTTA]TTTATTTATTTTTTT | 4215 |
| rs578133861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671052 | AGAATGCATGCAAGG[A/G]AACTGCATTAGGCTA | 4215 |
| rs578234504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632993 | GTGATATTGGGAGGC[C/T]GAGGCAGGCGGATCA | 4215 |
| rs578250497 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639689 | CCACATTTCTGGAAT[C/T]GCAGTCCTTATTTTG | 4215 |
| rs745319158 | in-del | -/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673545 | GAAATTCTACCTACC[-/T]TTGAAGCTCAAGCAC | 4215 |
| rs745343360 | snp | A/G | | | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63681823 | TTCCTGAGCGGCAGC[A/G]GCACATTGCCCGGCA | 4215 |
| rs745348368 | snp | A/C | 3.29745e-05 | 0.00406031 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691774 | TTACGGTGCTCTGAC[A/C]GAGAGCGTGACCCGA | 4215 |
| rs745349121 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636575 | GTCTGACAACTTAGT[A/G]TAGTGAAAAGAGTGC | 4215 |
| rs745354922 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673923 | AAAAAATAAAAAATA[A/G]ATAAAAATTATCCAG | 4215 |
| rs745367659 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671359 | CTCCCGGGTTCAAAC[A/G]ATTCTCTTGCCTCAG | 4215 |
| rs745382244 | snp | C/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686731 | ATAGCTAAATTTACC[C/G]GCCTCTCTATTCTTG | 4215 |
| rs745437961 | snp | A/G | 4.97319e-05 | 0.00498633 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691875 | AGGGTGAGCAGGGCC[A/G]GGATACATGGAGTCC | 4215 |
| rs745442111 | snp | C/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621090 | AAGGCAAAGCCACCA[C/G]TAAATGTTCTTAGTG | 4215 |
| rs745461789 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677532 | AGGGAAACAGCCAGG[C/T]ACATGGGTCTGTGAG | 4215 |
| rs745463659 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665251 | GCTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAT | 4215 |
| rs745476206 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638974 | GAGGTTGTAGTGAGC[C/T]GAGATCACTGCACTC | 4215 |
| rs745509910 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667030 | ACTATCTACCAGCCC[C/T]CCGAGCCCAGAAGCA | 4215 |
| rs745540664 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652006 | CTGTACGTTTTCTAC[C/T]TTATTTCCTAAATAA | 4215 |
| rs745642617 | snp | G/T | 1.64738e-05 | 0.00286995 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693815 | CGGTCGCCCTTTGCT[G/T]CATGGCAGGGGGCTG | 4215 |
| rs745670249 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663638 | AATTTGGATGAACTC[C/T]TTGAATATTGAGCAT | 4215 |
| rs745736315 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641041 | ATTCTGAAACACTTT[C/T]GGCCCCAAGAATTTT | 4215 |
| rs745751168 | snp | A/C | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692864 | TGAATAATGGCCCCC[A/C]CAAAGATGTCCACTG | 4215 |
| rs745762268 | snp | A/G | 0.000166761 | 0.00912977 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63646071 | AGCACAACGGGGAGA[A/G]GCGGTAAGTCTGCCT | 4215 |
| rs745826263 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642139 | TCATGGAAGCTTGTA[A/C]GGCTGTCATGGCATC | 4215 |
| rs745827023 | snp | A/G | 1.80546e-05 | 0.00300449 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652518 | AACCCTACGTTTTAA[A/G]TATACAATTAACCAA | 4215 |
| rs745832018 | in-del | -/CCT | 3.61422e-05 | 0.00425086 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681747 | CTCTGTTGTTGAAAG[-/CCT]CCTTTATGTGCTCTA | 4215 |
| rs745852412 | in-del | -/AAAC | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629580 | AAGGAAAAAAAACAA[-/AAAC]AAACAAAACCTCAAT | 4215 |
| rs745852966 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677460 | TTGTGACATGATAAG[A/G]CTTAGGAAAACCATC | 4215 |
| rs745930312 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667827 | GTGGTTGGTTGAATC[C/T]ACAGATGCAGAACCT | 4215 |
| rs745987896 | snp | A/G | 1.6504e-05 | 0.00287258 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634827 | AGATTACCTGTTAAA[A/G]CCAAAATGTACTTTT | 4215 |
| rs745993881 | snp | C/T | 1.6557e-05 | 0.00287719 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693530 | GGCTGAGGGGTGACA[C/T]GGGGTTCTCTCTTTC | 4215 |
| rs746012546 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629512 | GTCTCAGTCCATACC[A/G]CAGAGATAACTGGCT | 4215 |
| rs746025709 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646735 | TGGGAAGCCAAGGTA[C/G]AAGTTCTCAGTAGAA | 4215 |
| rs746040426 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680230 | TTGTTGAGGGATGGT[A/G]CTACTCTATTCCTGG | 4215 |
| rs746041567 | snp | A/T | 1.64901e-05 | 0.00287137 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685474 | GGTCACTGGGGGGAA[A/T]TGGGGCTGGGGGTGT | 4215 |
| rs746051778 | in-del | -/TGATA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631405 | ATTTCCAAGGGACAG[-/TGATA]AAGGGTAGAAGATAG | 4215 |
| rs746116187 | snp | C/T | 1.65307e-05 | 0.0028749 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688522 | TTTCTTTTTGTTTTC[C/T]CCAGCCCATCCTTCC | 4215 |
| rs746135030 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666657 | GTTTTGCAGATTATT[A/G]CAGGAATGCCTGTTA | 4215 |
| rs746135992 | snp | A/G | 3.33278e-05 | 0.00408201 | intron-variant, synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634714 | GTTTTTAAAGAAAAA[A/G]CACAACAGCAGCAGC | 4215 |
| rs746153464 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680925 | CAAATGTAAAAATAC[C/T]TTGTGGAATGATTGC | 4215 |
| rs746218252 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659777 | ACCTTGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 4215 |
| rs746218636 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644612 | CACATAAGCAAAAGC[G/T]CTTTGGGGTCTTTAA | 4215 |
| rs746227242 | snp | A/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694691 | ATGGACGACACGGTC[A/G]GGGCATCTGGCCTGG | 4215 |
| rs746254307 | snp | C/T | | | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696122 | TCCGCACTCTGCCAC[C/T]CTCCTGCCCCTTCCA | 4215 |
| rs746273875 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666969 | CCACTCTGGGGTGTC[C/T]AGACAGGTGCGGATC | 4215 |
| rs746292640 | snp | C/G | 1.87989e-05 | 0.0030658 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689714 | GCCCTCTCTGTGCAG[C/G]AGAGGAATGTGCCAA | 4215 |
| rs746405970 | snp | C/T | 1.69413e-05 | 0.00291039 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690247 | CAAAGTAACTCTTTC[C/T]TTCTGCTCTCCTGTA | 4215 |
| rs746433446 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661549 | ATCTTCCACTGTCAT[-/A]AAGTAATATCAAGCT | 4215 |
| rs746468402 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622219 | ATTGGTTCATCGTGT[A/G]GTGCTGATGATTAGC | 4215 |
| rs746560963 | snp | A/C | 1.74598e-05 | 0.00295459 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652525 | CGTTTTAAGTATACA[A/C]TTAACCAACCTTTCT | 4215 |
| rs746574398 | snp | A/G | 0.000215719 | 0.0103833 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691882 | GCAGGGCCAGGATAC[A/G]TGGAGTCCCCAGGAC | 4215 |
| rs746585875 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624529 | TATAAGTGTGTGAGT[A/G]TATGGAGACCAATGA | 4215 |
| rs746602493 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652922 | AATCAGGTATGGTAC[C/T]AGGGCTAGGGCTTAT | 4215 |
| rs746608353 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636799 | CGGCTGTGGGAGAAG[A/T]GGCTGAGGTGGTATG | 4215 |
| rs746609337 | in-del | -/TC/TCAAAACAT | 4.94542e-05 | 0.00497243 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685636 | GCATAGGCATTTTTG[-/TC/TCAAAACAT]GAATTGATGGGTTGA | 4215 |
| rs746616045 | snp | A/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687012 | TGGTGATGATTAAGG[A/T]GAAAGAAAGATGCCT | 4215 |
| rs746666485 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638339 | GAGAGAAATCAGTAC[A/G]GAATCAGAGCGAGGA | 4215 |
| rs746700251 | snp | A/G | 1.65553e-05 | 0.00287705 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692311 | CCAGCAAACGCCTGC[A/G]GACGATCTGTATGTC | 4215 |
| rs746707247 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634948 | GTGTTCAGTGCTTCT[A/C]GTCACCATTTCTCAC | 4215 |
| rs746707820 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673118 | TTGCATTGATGGGGA[A/G]GCGCAGGGTAGCCCA | 4215 |
| rs746807838 | in-del | -/GTT | | | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696218 | GAACCTGCAGCCATA[-/GTT]GTTATTTGACTATAT | 4215 |
| rs746868574 | snp | C/T | 1.65029e-05 | 0.00287248 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691156 | AACTTGCAGCATGAG[C/T]GCATCGTGCAGTACT | 4215 |
| rs746868904 | snp | A/C | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678654 | TCTCCAATACCAGTT[A/C]AGTGGTGAATTCTCA | 4215 |
| rs746879747 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627908 | TATTTTCTTCAATCC[-/T]TTTTTTTTTTTTCTG | 4215 |
| rs746926681 | snp | C/T | 3.44157e-05 | 0.00414809 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652679 | GGCAGATGGATGGGG[C/T]AGGGACAAGAGGGGC | 4215 |
| rs746953248 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629258 | CTCCCAAGTAGCTGG[C/G]ATTACAGGCGCACAC | 4215 |
| rs746986415 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665437 | CCCAAAGTGCTGGGA[C/T]TATAGGCATGAGCCA | 4215 |
| rs747061434 | snp | A/G | 1.65282e-05 | 0.00287469 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693656 | AGCCCACCAATCCTC[A/G]GCTGCCCTCCCACAT | 4215 |
| rs747073685 | snp | A/G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640006 | ATACCGGAGGTCTTT[A/G/T]AGAGGAGAATTGAAA | 4215 |
| rs747098862 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691613 | CTGGCAAAATGCCCT[A/G]CCCAGCCAGATAGGA | 4215 |
| rs747155622 | snp | C/T | 1.70869e-05 | 0.00292286 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693800 | CGGCCACACAGCTGC[C/T]GGTCGCCCTTTGCTG | 4215 |
| rs747155850 | snp | A/T | 1.66037e-05 | 0.00288125 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690271 | TCCTGTAGCTCCCAG[A/T]GCCCCCATCAACTGG | 4215 |
| rs747215645 | snp | A/C | 1.65113e-05 | 0.00287322 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634838 | TAAAGCCAAAATGTA[A/C]TTTTAAATCTGCTAC | 4215 |
| rs747221448 | snp | C/T | 3.30082e-05 | 0.00406239 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688756 | GCTCACATTGACCTA[C/T]CCAGAAGCCAGTGAT | 4215 |
| rs747235726 | snp | A/T | 1.66236e-05 | 0.00288297 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63646050 | GTGACGTCAGAATCA[A/T]GTTCGAGCACAACGG | 4215 |
| rs747276185 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654753 | TTATAAAAGAAATAG[A/G]TGGCTAGGTGCAGTG | 4215 |
| rs747356342 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631652 | TGGACTGGTTTGTGT[C/T]CTGGGTTTTGGCCAG | 4215 |
| rs747479854 | snp | A/C | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694736 | CCAGAGAGCCCGAGG[A/C]GGTGTCTCAGGCTGC | 4215 |
| rs747489346 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660178 | AGCAGTTGCCTCACC[A/G]CCTTTTGTTACCACC | 4215 |
| rs747585379 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646987 | CAGGTGAAGAGCATA[C/T]CCATTAGTATGAGGT | 4215 |
| rs747588673 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650710 | GTTTTTTTTTTTTTT[-/A]AGACAGGGTCTCATT | 4215 |
| rs747669813 | snp | C/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696484 | TCAGTCCAGAGGTGT[C/G]TGCCCCTTTCCTCCA | 4215 |
| rs747700437 | snp | C/T | 3.60179e-05 | 0.00424354 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689570 | TTTCCCCGAATACGG[C/T]GTCATCAAGGCAACT | 4215 |
| rs747742093 | snp | C/T | 1.65252e-05 | 0.00287443 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657834 | ATGATCTTGATAAAG[C/T]AATTGACATTTTAGA | 4215 |
| rs747751723 | snp | C/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674781 | GGAGATGAATCGAGT[C/G]CAGGTAGAGGGTTTA | 4215 |
| rs747808129 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624638 | GTCCCCACATCAGTT[A/G]TCCTCCTGTCAGTTT | 4215 |
| rs747812947 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665252 | CTCACTGCAAGCTCC[A/G]CCTCCCAGGTTCATG | 4215 |
| rs747867118 | snp | A/G | 3.49321e-05 | 0.00417909 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689679 | CCCGTGGGCGCCTGC[A/G]GAGTGCGGACAGCGA | 4215 |
| rs747912271 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638529 | ATTGTCAGTTATTCC[C/T]GTTGCTCCTGCTGAG | 4215 |
| rs747980360 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688538 | CCAGCCCATCCTTCC[A/G]GAAATCACGAATGTC | 4215 |
| rs747980771 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666450 | TCCAGCCTGGGCAAC[A/C]TAGCAAGACTCTGTA | 4215 |
| rs748003047 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623424 | TAGAATTCACATCCT[A/G]CTTTTTGAAAAATCC | 4215 |
| rs748040793 | in-del | -/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680577 | AGCTCTTGGGCTAGG[-/T]AGGAAGGAGGACCTG | 4215 |
| rs748062558 | snp | C/T | 1.65367e-05 | 0.00287543 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691263 | AATGCATGTGAGACA[C/T]ACACAAAAGAGGGCC | 4215 |
| rs748064493 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653181 | CTCACTCCACCCCAA[C/T]GGTCCTTATTTACTT | 4215 |
| rs748109392 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685553 | GCAGAAAATTCCTTG[C/T]CTGGAAGCTGCCAAT | 4215 |
| rs748202724 | in-del | -/CTT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637620 | GAGCTTTGGGGAAAG[-/CTT]CTAACTACAACTGTC | 4215 |
| rs748260060 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677610 | CTAAACCTCCATCTT[A/G]TCTTTGCCTACAAAC | 4215 |
| rs748275986 | snp | C/T | 1.65209e-05 | 0.00287405 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667055 | GAAGCAGGCACCTCT[C/T]TGTCAGTGAGTATTT | 4215 |
| rs748311399 | in-del | -/GGGTGGGGCCTGGCCCT | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695557 | CTCGGCCCTTGCCCA[-/GGGTGGGGCCTGGCCCT]CATCTTGACCAAAGC | 4215 |
| rs748311467 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653151 | CTCCAATAAGTTCTT[C/T]AACTCCTCCTCCTCC | 4215 |
| rs748382557 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634588 | AAAAAGGATTGACTG[-/T]TTAGGAAGTAATCTT | 4215 |
| rs748388819 | snp | A/G | 1.72967e-05 | 0.00294076 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646125 | TATGCCAAAGTTCTC[A/G]GATAGCATTGAGTTC | 4215 |
| rs748404733 | snp | A/G | 1.65633e-05 | 0.00287774 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690403 | TCCAGACAGTCCTGA[A/G]ACAAGCAAGGTACAC | 4215 |
| rs748426375 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634509 | GATGAGGGAAGTCTT[A/G]ATCTTTTGCTGTGCC | 4215 |
| rs748429549 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656755 | GTACCCTCAGGGACC[A/T]TCTATTTAATATTTC | 4215 |
| rs748453035 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669425 | TGGAAGCCACTGAAA[A/G]TGTTTGCCCCTTATA | 4215 |
| rs748513456 | in-del | -/AGTA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668333 | CAGGCAAGTACTGGT[-/AGTA]AGTAAGTATTGCCAG | 4215 |
| rs748573984 | snp | A/T | 1.68213e-05 | 0.00290006 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634681 | CGAAGGATACAAATT[A/T]TTAACCTCAGTTTTT | 4215 |
| rs748619045 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634399 | GAAGGCCCAAAAGGA[C/T]GAGGCTGGGAAAAGG | 4215 |
| rs748699911 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684226 | AAGAACGTCATTTTT[C/T]ACAAGAGCGTTCACA | 4215 |
| rs748765124 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642870 | TCAAGCAATCCTCTT[C/G]CCTCAGCTTTCCAAG | 4215 |
| rs748881884 | snp | A/G | 1.65201e-05 | 0.00287398 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657849 | CAATTGACATTTTAG[A/G]TAGAAGCTCAAGCAT | 4215 |
| rs748895630 | snp | C/T | 1.67413e-05 | 0.00289316 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691682 | GGAATGGGCTTGCCC[C/T]TCCACCAGCCCTCCC | 4215 |
| rs748915853 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661858 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 4215 |
| rs748950373 | snp | C/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689463 | CGCCTTGTAGCCCGG[C/G]GTGTCTCAGACCTGG | 4215 |
| rs748978772 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648956 | TACCTTCTTGAGATG[A/T]TAGGCTTTGCGTGAA | 4215 |
| rs749057766 | in-del | -/A | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687518 | TTCCGTCTCAAAAAG[-/A]AAAAAAAAAAAAGCA | 4215 |
| rs749143580 | in-del | -/AA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634444 | ACTGATGGTTCCTTG[-/AA]AAGGAGGATTCCTTT | 4215 |
| rs749150693 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626443 | GTTAATTTCACTAAA[C/T]GTTAAAATGTAGTGG | 4215 |
| rs749192616 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688566 | GTCCCGTGCCCAGAG[C/T]TTCCCTGACAACAGA | 4215 |
| rs749203345 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639792 | TGGAAAGTTGTAGGA[A/G]ATCAGTGGAAGAGAT | 4215 |
| rs749215418 | snp | G/T | 1.64792e-05 | 0.00287042 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688782 | GTGATTCCCCTGTCT[G/T]ACTCAGATCGGGAAA | 4215 |
| rs749356779 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629365 | CCTGACCTCAAGTGA[G/T]CCACGCATCTTGGCC | 4215 |
| rs749378470 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679893 | AAAACTGGTCTGGAC[C/T]AGGGATCTATCATCA | 4215 |
| rs749421477 | snp | C/G | 1.65124e-05 | 0.00287331 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632842 | AGTGAGATTTGTTGG[C/G]GAGGGGTTTTCAAAT | 4215 |
| rs749446678 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658035 | AGCATAAGCACAGCA[A/C]AGCCCACTTGTCAGT | 4215 |
| rs749482716 | snp | G/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693833 | TGGCAGGGGGCTGCT[G/T]CTGGGCTCAGTGAAG | 4215 |
| rs749490312 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628638 | GTGCTGGGATTACAG[A/G]CGTGAGCCCCTGGGC | 4215 |
| rs749494387 | snp | A/C | 1.65078e-05 | 0.00287291 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691150 | CTAAAGAACTTGCAG[A/C]ATGAGCGCATCGTGC | 4215 |
| rs749547349 | snp | C/T | 1.76693e-05 | 0.00297226 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63681796 | GCCGAAGCTCACCTC[C/T]CCCTGGCTATGTTCC | 4215 |
| rs749557806 | in-del | -/AGA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667459 | TGCTTATGATTCCTG[-/AGA]AGAAGTCTTTATACT | 4215 |
| rs749588352 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620972 | GATCGCGCCACTGCA[C/T]TCCAGCCTGGACGAC | 4215 |
| rs749636744 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656912 | AACTTACAATCATGA[C/T]GGAAGGGAAAGCAAA | 4215 |
| rs749692883 | snp | A/G | 6.64088e-05 | 0.00576194 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692333 | CTGTATGTCGGGGAC[A/G]GGCATGCGCTCCGTC | 4215 |
| rs749800528 | snp | G/T | 1.68015e-05 | 0.00289836 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634692 | AATTATTAACCTCAG[G/T]TTTTTTGTTTTTAAA | 4215 |
| rs749817590 | snp | C/G | 3.50171e-05 | 0.00418417 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689597 | AACTTGTTCACCCTG[C/G]TGCCCTCCAGCCGCT | 4215 |
| rs749837279 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636131 | GATTGTTTGGGTGCC[A/G]AGGCCTGGAAGAACT | 4215 |
| rs749837978 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671132 | TGGAGAGAGGAAGGA[A/G]CAGGTGAACTTGTGA | 4215 |
| rs749850994 | snp | G/T | 3.59202e-05 | 0.00423778 | missense, downstream-variant-500B, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681896 | AGAGACCAGCGAGCA[G/T]TGCGTGAGTATAGGG | 4215 |
| rs749883353 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632790 | CAAAGACACAGGTCA[C/T]TCAAATAGGCAGGTG | 4215 |
| rs749910024 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667259 | TGACTCTCAAGGAAC[C/T]TAAAATATAATGATA | 4215 |
| rs749929711 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652831 | TTTTTTACTACATGG[G/T]AGATTACTCAGCCAT | 4215 |
| rs749971743 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653856 | ACCAACACCGCTATC[A/T]AATTCCAGAACATTT | 4215 |
| rs749990089 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660766 | CCGCCTAATTTTGTA[-/T]TTTTTTTTTAGTAGA | 4215 |
| rs749990895 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629038 | GAGGTTTGGAGAGAA[C/T]AAATGATTTGCTCAG | 4215 |
| rs750016141 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679680 | ATGGGGTCTCACCAT[A/G]TTGCCCATGCTGGTC | 4215 |
| rs750104604 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666103 | CAAAGGCCCCCCTTT[C/G]TTGCTTAGTTTTCTC | 4215 |
| rs750177517 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694312 | CCCCTAGAGTCCCAG[C/G]TTGGCTCTGCCAGTC | 4215 |
| rs750213086 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678395 | CTGTTTGAGACCATT[A/G]CAAAGGCATGGCTCA | 4215 |
| rs750283630 | snp | A/G | 1.67421e-05 | 0.00289323 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652652 | TACATTACATGAACA[A/G]TGAGGTGAGAAGGCA | 4215 |
| rs750289116 | snp | A/C | 1.73021e-05 | 0.00294121 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689663 | GTGCAATACCTGGAC[A/C]CCCGTGGGCGCCTGC | 4215 |
| rs750297384 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645244 | GGAGACGGAGGTTGC[A/G]GTGAGCCGATATTGT | 4215 |
| rs750305812 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671993 | ATCATTTAAAAAAAA[A/G]AAAATGAGGCCAGGT | 4215 |
| rs750330847 | in-del | -/TTG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634064 | TTTAAAAAGCTGCTT[-/TTG]TTGTTGTTACCTTAT | 4215 |
| rs750330867 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659431 | GATCCAAAATTGCTC[C/T]GTGCTCAGGAATCCT | 4215 |
| rs750405354 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657629 | ACATTTAGAGAAAAA[A/G]ATCTGTATGGTTTCA | 4215 |
| rs750413926 | snp | A/C | 1.66596e-05 | 0.00288609 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692356 | GCTCCGTCACTGGCA[A/C]ACCCTACTGGATGAG | 4215 |
| rs750413982 | snp | A/G | 5.71946e-05 | 0.00534734 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689546 | TGCACCCTTTCAGGC[A/G]GAAGAACATTTCCCC | 4215 |
| rs750420240 | snp | C/G | | | missense | MAP3K3 | GRCh38.p7 | 17:63693557 | TTTCCAGGAGCCTGG[C/G]CTGCACTGTGGTGGA | 4215 |
| rs750471899 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632471 | CACTCCAGCCTGAGT[A/G]ACAGAGCAAGACCTT | 4215 |
| rs750473930 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650004 | CTTCTTCCTCTCAGC[A/T]TGGAAGAGGACAAGA | 4215 |
| rs750524311 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683959 | GTCAGGAGTTCAAGA[C/T]CAGCCTGGGCAACAT | 4215 |
| rs750589254 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661308 | CGCCTCAGCTTCTCA[A/T]AGTGCTGAGATTACA | 4215 |
| rs750611728 | snp | A/G | | | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695975 | GGTGACCTGGGCCCA[A/G]AGGTTCTGAAGGGCA | 4215 |
| rs750612412 | in-del | -/CTC | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633866 | CTAACCTCCTTTCTT[-/CTC]ATTTGCACCTTGTTT | 4215 |
| rs750630823 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662805 | TGGGATTACAGGCGT[A/G]CGCCACTACGCCCGG | 4215 |
| rs750667747 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647903 | CACAGGAAAGAGGAA[A/G]GAAGTCATGACTTTT | 4215 |
| rs750732393 | snp | A/G | 9.3576e-05 | 0.00683954 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622784 | TGTCGCCACCGCCCC[A/G]GCCTGTGCCCGCGCT | 4215 |
| rs750761927 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684148 | TGTCTCGAACAACAG[C/T]ACCAACAACAAAATG | 4215 |
| rs750779438 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624116 | GAGGGAAGGTCTGCT[C/G]TGAGAGTGGACATAA | 4215 |
| rs750786564 | snp | C/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675430 | GACAACTTCCTGACT[C/G]CATCAGCTTCCTGAT | 4215 |
| rs750869380 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625835 | CCAGCACTTTGGGAA[A/G]CTGAGACTGGTAGAT | 4215 |
| rs750905700 | snp | C/G | 1.69585e-05 | 0.00291187 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646106 | ATGAGTAGCTGTGTT[C/G]ATGTATGCCAAAGTT | 4215 |
| rs750910034 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639007 | GCCTGGGCGACAGAG[C/T]AAGACTCCATCTCAG | 4215 |
| rs750929203 | snp | A/C | 6.59152e-05 | 0.00574049 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688838 | AGGTGGAACCTACCC[A/C]CGGCGCTACCACGTG | 4215 |
| rs750932299 | snp | A/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674347 | AGGTGGGTGGATTGC[A/T]TGAGCCCAGGAGTTC | 4215 |
| rs750933927 | snp | C/T | 6.70354e-05 | 0.00578906 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646026 | CTGTCTATCATTCTT[C/T]TTGGCAGAGTGACGT | 4215 |
| rs751026465 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632000 | CTGACACTGTGCCAT[-/A]ATCCTCTCTCTATGG | 4215 |
| rs751073898 | snp | A/G | 1.70667e-05 | 0.00292114 | missense, intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692398 | TCAGCGGCGAGGGCT[A/G]TGGAAGGAAAGCAGA | 4215 |
| rs751084242 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640424 | ATGTGTATGTGTGTA[C/T]GTTGATTTTTGCAGG | 4215 |
| rs751088841 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655403 | ATCAGTGAGGGCTGC[A/G]GTTTCTCCACCATCC | 4215 |
| rs751109085 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690768 | TTCACTTGGTCCAGC[C/T]CTAGAGGAGGAATCA | 4215 |
| rs751148786 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667348 | TGCTTGAAGACTTCC[A/G]GCTGTGTTTACACTC | 4215 |
| rs751232193 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654003 | ACCCAAGTAGCTGGG[A/T]CTACAGGCACACACC | 4215 |
| rs751237151 | snp | A/C/T | 6.73418e-05 | 0.00580234 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634675 | GTTGCACGAAGGATA[A/C/T]AAATTATTAACCTCA | 4215 |
| rs751266659 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626762 | ATCTGACTCAGGGAC[A/G]CTGAAGCACAGACTC | 4215 |
| rs751301039 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681228 | CACGAAGGCCTTTTT[A/G]CCTGATACAAGTAGA | 4215 |
| rs751338768 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666235 | TGATAGCTTTTCCCA[A/G]TTGAACATGATCCTG | 4215 |
| rs751348276 | snp | C/T | 3.54227e-05 | 0.00420834 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657957 | ACAAAGCTTGCTTTC[C/T]TTCAGGAACTTGTCT | 4215 |
| rs751351617 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636917 | CCCAATTGGAGGCCT[A/G]TATGCGCTTCATCCA | 4215 |
| rs751360446 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630601 | CAAAGTGCTGGGATT[A/G]CAGGCATGAGCCACC | 4215 |
| rs751441762 | snp | C/G | 5.21463e-05 | 0.00510592 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689672 | CTGGACCCCCGTGGG[C/G]GCCTGCGGAGTGCGG | 4215 |
| rs751463902 | snp | C/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694573 | TCTGGGCTCTGAGTA[C/T]CCCTGCTTTGGGCTT | 4215 |
| rs751469833 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691944 | GGGGCCAATCACTTA[A/G]CCATTCTGAACTTTC | 4215 |
| rs751493085 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695483 | TGTTCCCCCAGGGGC[G/T]CTATCAGCCCCTGTA | 4215 |
| rs751513633 | snp | C/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694564 | TGTGTGCCCTCTGGG[C/T]TCTGAGTACCCCTGC | 4215 |
| rs751544538 | snp | A/T | 1.67086e-05 | 0.00289033 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657804 | CACAGCTCTCCATCC[A/T]GCTGAAAAACCAAGA | 4215 |
| rs751548322 | in-del | -/AAT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653270 | CCCAGCTCCAAGAAG[-/AAT]ATTACAGACTACAAT | 4215 |
| rs751553791 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679769 | GAGCCACTGCACCTG[A/G]CCACACATGAGTTTT | 4215 |
| rs751575395 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670881 | GGGAGGCAGAGCCTT[A/G]TGGACCCTGGTTAAG | 4215 |
| rs751588401 | snp | G/T | 1.71038e-05 | 0.00292431 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646119 | TTCATGTATGCCAAA[G/T]TTCTCAGATAGCATT | 4215 |
| rs751596578 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635443 | TAAAATGCTAAGATA[A/G]CTTTTCCTCTTAATG | 4215 |
| rs751686741 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620653 | GCAGGCTTAAGCTTG[C/T]TGGAAGAAAAAGAAA | 4215 |
| rs751718307 | snp | C/T | 4.94588e-05 | 0.00497262 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691826 | GAGGGCATGTCCTAC[C/T]TGCACAGCAACATGA | 4215 |
| rs751740583 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651541 | ACACACAAAAGTAGA[C/G]AGAGTATTAAACTGA | 4215 |
| rs751765508 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685279 | AGCCTCTGCTTTGCT[C/T]TCCTGCCAGAGCTCC | 4215 |
| rs751786963 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663832 | AGGAATTCCAGGCTG[C/T]GATGAGCTATGATTG | 4215 |
| rs751899532 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627360 | CTAAGTGTGTCAGAC[C/T]ACTCCCACTCTCAGG | 4215 |
| rs752020848 | snp | C/T | 3.44471e-05 | 0.00414999 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691080 | CCCTGAGAGCTGAGG[C/T]GACCACTGACCCCTC | 4215 |
| rs752024016 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650273 | ATTTGTTTAACTTTG[A/T]TGATGGCTTATTTTG | 4215 |
| rs752030368 | snp | A/C | 6.61288e-05 | 0.00574979 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652611 | GGAGCACAAGGTGAC[A/C]ACAGTATTTGGACAA | 4215 |
| rs752033758 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661511 | TTTCAGCTCTTGACC[C/T]TCTTAGGACTTTCTA | 4215 |
| rs752051678 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675636 | TGGCAGCTTAAACCC[C/T]GCTTTTCTCCTTCTG | 4215 |
| rs752053417 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692106 | CCCTTTGCTAAATCC[C/T]TTGCCCTTTGCAGTT | 4215 |
| rs752065475 | in-del | -/A | 1.64904e-05 | 0.00287139 | intron-variant, frameshift-variant, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634786 | GCAGGGGCCAGTGAG[-/A]AAAAAGAAATTTTTG | 4215 |
| rs752145696 | snp | A/G | 0.000146338 | 0.00855263 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690999 | CAACTGCAGTTCCCA[A/G]GGCAGATCCCTGTGA | 4215 |
| rs752161435 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641698 | CAGATACGTGGCAAG[C/T]AGATGAGCCTTGCTT | 4215 |
| rs752290095 | snp | A/G | 1.86621e-05 | 0.00305462 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692434 | GGTGAGCACTGGGAC[A/G]TGCAGAACCCATTCT | 4215 |
| rs752309701 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654984 | GAGGTTGCAATGAGC[C/T]GAGATTGCAGCTCAT | 4215 |
| rs752357350 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652050 | ACTTTTATTTAAGTT[A/C]TGGGGTACATGTGTA | 4215 |
| rs752393083 | snp | A/G | 1.64928e-05 | 0.00287161 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634770 | TAACAACAAGCTCAT[A/G]TGCAGGGGCCAGTGA | 4215 |
| rs752413223 | snp | G/T | 1.72502e-05 | 0.0029368 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645999 | GTGACACATTCCAGA[G/T]AATTCTCTAACCTGT | 4215 |
| rs752427098 | in-del | -/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666720 | TGGGGCACTAGGTCT[-/C]AGCGCTCATACATCA | 4215 |
| rs752434959 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692165 | TCTCCAGCAGCTCTC[A/G]GTGACCCGGGGGTGG | 4215 |
| rs752489765 | snp | C/T | 1.79732e-05 | 0.00299771 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622811 | CGCTGCTTCGCGACG[C/T]CCCGCCCCAGGCTGA | 4215 |
| rs752528601 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666916 | GTAAAGATGTAGCTT[A/G]GCCTTTTTCCTCTTC | 4215 |
| rs752583799 | in-del | -/AGAGTT/AGTG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650696 | GAGAGAGAGAGAGAG[-/AGAGTT/AGTG]TTTTTTTTTTTTTTA | 4215 |
| rs752617110 | snp | C/T | 1.64827e-05 | 0.00287073 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690332 | TTCGGCAGGGTCTAT[C/T]TGTGCTATGACGTGG | 4215 |
| rs752628018 | snp | A/C | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681575 | TAGTGCCTGCTCCAT[A/C]TCTGGAGTTTGTTTC | 4215 |
| rs752685930 | snp | A/C/T | 3.29599e-05 | 0.00405944 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667027 | AATACTATCTACCAG[A/C/T]CCCCCGAGCCCAGAA | 4215 |
| rs752694566 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632287 | ACTGGAGTCCAGGAG[A/T]TGGAGACCAGCCTGG | 4215 |
| rs752712800 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667644 | TCCCTGAAATAAAAT[A/C]GTGTAGTATTTGCAT | 4215 |
| rs752713759 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683629 | CGCCTGCCTCTTTAG[C/T]TGAAGAGAATTGCTC | 4215 |
| rs752776142 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657776 | TATTATTTTCCTTTT[C/T]TATGTCTTGTATCAC | 4215 |
| rs752865397 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637129 | AGCCTTAGAGTGTGT[G/T]TGCGTGCATGCGCAC | 4215 |
| rs752869491 | snp | A/G | 1.66324e-05 | 0.00288374 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652638 | ACAACCTCTTGATCT[A/G]CATTACATGAACAAT | 4215 |
| rs752889540 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644359 | AGCTGGGATTACAGG[C/T]GTGCGCCATTACTCA | 4215 |
| rs752896245 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672592 | TGTTATGTTGAAACC[A/G]TGCACCCAGGCGAGA | 4215 |
| rs752897281 | in-del | -/GA | 1.68117e-05 | 0.00289923 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646090 | GTAAGTCTGCCTTCT[-/GA]TGAGTAGCTGTGTTC | 4215 |
| rs752964120 | snp | C/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620767 | CCCAGCACTTTGGGA[C/G]GCCGAGGCTGGCGGA | 4215 |
| rs753079549 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651644 | TTAAATTTTGCTGAA[A/G]TATTTAATAACAAAT | 4215 |
| rs753092392 | in-del | -/A | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674080 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 4215 |
| rs753104643 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690584 | AGGACTGTGGTCTGA[A/G]GAGCACCAAGCACCT | 4215 |
| rs753124211 | in-del | -/CAGGG | 1.65627e-05 | 0.00287769 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692209 | AAATGCAAGAGGGTC[-/CAGGG]TTGCAGCCTCTGCCC | 4215 |
| rs753161204 | snp | C/T | 0.000100521 | 0.00708875 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688494 | TGCTGTGGAAGTGTG[C/T]GGGAGTCTGTTTTTT | 4215 |
| rs753162441 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635676 | TGGTGATATTAATAA[C/T]CATTTAACATCGGAT | 4215 |
| rs753174076 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691191 | CTGTCTGCGGGACCG[C/T]GCTGAGAAGACCCTG | 4215 |
| rs753235898 | snp | C/T | 3.36185e-05 | 0.00409977 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691094 | GCGACCACTGACCCC[C/T]CCCCTAGGAGGTGAG | 4215 |
| rs753254499 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675695 | GCCTCTCTCTGAACA[A/G]TGGAACTGCTACTGT | 4215 |
| rs753261405 | snp | G/T | 1.82297e-05 | 0.00301903 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681924 | GGGGGGCTGGGATAT[G/T]CCTGTGGCCTGTATC | 4215 |
| rs753265487 | in-del | -/TTCT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693311 | ACAGTTATTGTAGAG[-/TTCT]TTCTGTCAAGTCTAA | 4215 |
| rs753275890 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650433 | CAGCCTCCCAAGTAG[C/G]TGGGATTGCAGGGCA | 4215 |
| rs753280027 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665079 | AGGCCAAGGCAGGCA[G/T]ATCACCTGAGGTCAG | 4215 |
| rs753340348 | in-del | -/AA | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695378 | GGTGACGGACGCCTC[-/AA]GAGAGAGAAGAGAAA | 4215 |
| rs753392380 | snp | A/G | 1.69012e-05 | 0.00290694 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690969 | CTAGACAGTTAAGAG[A/G]GTCCCCCTTTTCTCC | 4215 |
| rs753431133 | snp | G/T | 1.71302e-05 | 0.00292657 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690236 | AATAATGTACACAAA[G/T]TAACTCTTTCCTTCT | 4215 |
| rs753435082 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693424 | TCCAAGCTGAGGTAT[C/T]CCTCAGCTTGGCCTG | 4215 |
| rs753465322 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651845 | GGGAATTCCTGTGAC[C/T]CTGTAGTAGAAAATC | 4215 |
| rs753506678 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627678 | AACTCCTGACTGCAG[C/G]TGATCCACCCTCCTC | 4215 |
| rs753529653 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620526 | ATGACGTGCCTGTTA[C/T]ATTGATAAATACTAA | 4215 |
| rs753532238 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650135 | ATTTCTCCAGTCACA[C/T]TGGGCATCTTTTCAT | 4215 |
| rs753609421 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660633 | GTTTCACTCTTGTTG[A/C]CCAGGCTGGAGTGCA | 4215 |
| rs753706365 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688860 | TACCACGTGTCTGTG[C/T]ACCACAAGGACTACA | 4215 |
| rs753715402 | snp | A/G | 1.66194e-05 | 0.00288261 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632646 | TGCTGGTCTGTATTT[A/G]AGTGTCTTAGTCCAT | 4215 |
| rs753725999 | snp | C/T | 1.6546e-05 | 0.00287624 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692223 | CCAGGGTTGCAGCCT[C/T]TGCCCTTTCATGCCT | 4215 |
| rs753750917 | snp | G/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685201 | AGGCTCAGCAGGGTA[G/T]TACCATCTCCAGCGC | 4215 |
| rs753770815 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669060 | GGGTTGAAGAACCCC[A/G]GGGGCTTTGCACTGT | 4215 |
| rs753831759 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632756 | GTCACCGGATGCCTG[C/G]ATATGAGACCATGAA | 4215 |
| rs753855457 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670684 | GCCAGGAAAGCCTTA[A/G]GCATGAATGGGATTT | 4215 |
| rs753892625 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661051 | CTGAGTTTTGGTAAT[C/T]ACAGAACTATCTCTT | 4215 |
| rs753912095 | in-del | -/AAC | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680032 | TCTGAAACAAAACAA[-/AAC]AACAAAACAGAATAG | 4215 |
| rs753922082 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631141 | AAAATACAAAAATTA[A/G]CAGGGCATGGTGGTG | 4215 |
| rs753964127 | snp | A/G | | | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695874 | AAAAACTGTGGACAT[A/G]CTGGCTCAGCATCCT | 4215 |
| rs754004595 | in-del | -/TTTCTG | 1.7094e-05 | 0.00292348 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652540 | ATTAACCAACCTTTC[-/TTTCTG]TTTCTTTTCAGAATT | 4215 |
| rs754006982 | snp | A/G | 5.16364e-05 | 0.0050809 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657787 | TTTTCTATGTCTTGT[A/G]TCACAGCTCTCCATC | 4215 |
| rs754007278 | in-del | -/T | 1.65751e-05 | 0.00287876 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693514 | CTGGGAGTCCAGGGC[-/T]GGCTGAGGGGTGACA | 4215 |
| rs754016866 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647864 | AGTATTTATCTAAAT[A/G]TAGGCCCTTATAGAA | 4215 |
| rs754128161 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640469 | TCTGCAGTTCTGAGA[C/T]CCAAACAGTACTACA | 4215 |
| rs754128532 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645975 | AAGGCTTACTTGGCA[A/G]TGGCAGGAGTGACAC | 4215 |
| rs754141901 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651604 | TACTAACATTTTCCC[A/T]GTCTTGTTTTATCAA | 4215 |
| rs754210174 | snp | A/G | 1.69539e-05 | 0.00291147 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646013 | AGAATTCTCTAACCT[A/G]TCTATCATTCTTTTT | 4215 |
| rs754221571 | snp | C/T | 6.60807e-05 | 0.0057477 | synonymous-codon, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693618 | GTATGAAGCTATGGC[C/T]GCCATCTTCAAGATT | 4215 |
| rs754226212 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637673 | AGGATTAAGGTTTTT[C/T]TCTCTTTATGGGATT | 4215 |
| rs754231861 | snp | A/G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666002 | CTGAGCTCTCACCCC[A/G/T]ACTCTCACCAGTGCC | 4215 |
| rs754263410 | in-del | -/TCAG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631286 | GAGTGAAACCCTGTT[-/TCAG]TCAGTCAGTCAATCA | 4215 |
| rs754283031 | snp | C/T | 1.66721e-05 | 0.00288717 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691710 | CCCCTGAGGGGACTC[C/T]TCTGACTTCTTGTGG | 4215 |
| rs754301618 | snp | G/T | 3.30366e-05 | 0.00406413 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688618 | CACAGAGCCTGGGTG[G/T]GTAATGCAGGGTGTC | 4215 |
| rs754354108 | snp | C/T | 0.00092926 | 0.0215352 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688510 | GGGAGTCTGTTTTTT[C/T]TTTTTGTTTTCTCCA | 4215 |
| rs754404166 | snp | G/T | 1.64914e-05 | 0.00287149 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634797 | GTGAGAAAAAGAAAT[G/T]TTTGGTAAGGATCCA | 4215 |
| rs754420338 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652767 | ATCATCTGCAGGTTT[G/T]CATTTTCTAGACCCC | 4215 |
| rs754446404 | snp | A/G | 0.000108417 | 0.00736184 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689568 | CATTTCCCCGAATAC[A/G]GCGTCATCAAGGCAA | 4215 |
| rs754460824 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685291 | GCTCTCCTGCCAGAG[C/T]TCCTTGGGATGCCAG | 4215 |
| rs754461418 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668147 | CCTTATCCATATAGG[C/T]AGAATTGCTTCAAAT | 4215 |
| rs754476349 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640557 | GACTCATTTGGCAAC[A/C]AGACCTGTCCTGAAT | 4215 |
| rs754509552 | snp | A/G | 1.73096e-05 | 0.00294185 | missense, intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692407 | AGGGCTATGGAAGGA[A/G]AGCAGACGTGTGGTG | 4215 |
| rs754533496 | snp | A/G | 1.73899e-05 | 0.00294867 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689673 | TGGACCCCCGTGGGC[A/G]CCTGCGGAGTGCGGA | 4215 |
| rs754582789 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654069 | AGGCAGGGTTTCACC[A/G]TGTTGCCCAGGCTGG | 4215 |
| rs754638634 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692315 | CAAACGCCTGCAGAC[A/G]ATCTGTATGTCGGGG | 4215 |
| rs754663581 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689460 | TTCCGCCTTGTAGCC[C/T]GGGGTGTCTCAGACC | 4215 |
| rs754775264 | snp | C/T | 1.65162e-05 | 0.00287365 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691241 | TGCCAGGGGTACGTG[C/T]CCCTTGAATGCATGT | 4215 |
| rs754796483 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666903 | TAGGCCTGACTGTGT[A/G]AAGATGTAGCTTGGC | 4215 |
| rs754820841 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646242 | CCTTGTCTTGGCCTA[C/G]TAATTGAACCTTGTT | 4215 |
| rs754833029 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663274 | TTGGGAGGCTGAGGT[A/T]GGTGGATCCCTTGAG | 4215 |
| rs754910847 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629281 | GCGCACACCACCACG[C/T]GCAGTTAATTTTTTT | 4215 |
| rs754924253 | snp | A/G | 1.6628e-05 | 0.00288335 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657810 | TCTCCATCCTGCTGA[A/G]AAACCAAGATGATCT | 4215 |
| rs754942033 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666286 | CTGGAATCTTCTTAA[G/T]TTTCAGGGAGTGATT | 4215 |
| rs755005880 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630955 | AGAGGGCATATAGGG[C/T]ACCAGAGCAGATTTC | 4215 |
| rs755012843 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681414 | ATGGCATTAGTGCTC[C/T]AGAGGAAGAGAGAAG | 4215 |
| rs755103678 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634457 | TTGAAGGAGGATTCC[G/T]TTTTAGGACTCCTTC | 4215 |
| rs755109399 | snp | C/T | 1.65351e-05 | 0.00287528 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652613 | AGCACAAGGTGACAA[C/T]AGTATTTGGACAACC | 4215 |
| rs755128911 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637398 | CTGATTCCTAGTCAC[C/T]GTAATTTTACCATGT | 4215 |
| rs755130371 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669273 | AGAGGGCTTTTAGAC[A/T]ATGTCTGTGGAGAGC | 4215 |
| rs755152020 | snp | C/T | 1.66269e-05 | 0.00288326 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63646054 | CGTCAGAATCAAGTT[C/T]GAGCACAACGGGGAG | 4215 |
| rs755202684 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685328 | ATTTTTCTCCCTCCT[A/G]GAAACTTGCCTTTCA | 4215 |
| rs755290666 | snp | G/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670918 | ATCATTGCATGGAAA[G/T]TAGTGAAAAGCTACT | 4215 |
| rs755299577 | in-del | -/CTGT | 0.000510178 | 0.0159634 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646011 | AGAGAATTCTCTAAC[-/CTGT]CTATCATTCTTTTTG | 4215 |
| rs755335974 | snp | A/C/T | 5.38212e-05 | 0.00518731 | missense, synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63681776 | TCTAGGCTCCCAGAA[A/C/T]CCTGGCCGAAGCTCA | 4215 |
| rs755427746 | snp | A/C | 1.64947e-05 | 0.00287177 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632820 | GTGTGTGACCCTGGC[A/C]GAGCTAAGTGAGATT | 4215 |
| rs755494718 | snp | C/G | 5.84744e-05 | 0.00540683 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691004 | GCAGTTCCCAAGGCA[C/G]ATCCCTGTGAGGCCA | 4215 |
| rs755506103 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661641 | TTGTTACCTCATATT[C/T]GCGTTGACAAAAATA | 4215 |
| rs755526432 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668272 | AGTTACAGGAAAAAT[A/G]TGTTTCTGAGGTACT | 4215 |
| rs755535835 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656441 | AACCCAGTCTCTACT[-/A]AAAAAAAAAAAAAAT | 4215 |
| rs755569980 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648395 | TGAAGAAGGAGGGGT[A/G]TGATTTGCTATTAGG | 4215 |
| rs755581457 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671008 | AAGATTGATCTGGCT[A/G]CAGTGTGGATAACAG | 4215 |
| rs755591193 | snp | C/T | 1.72273e-05 | 0.00293485 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690226 | GATATTCATAAATAA[C/T]GTACACAAAGTAACT | 4215 |
| rs755708063 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666950 | TACAGAACAGTTCCT[C/T]TCCCCACTCTGGGGT | 4215 |
| rs755713679 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640655 | AAATTAGGATAGCTT[C/T]GATAAAAAGCATGTA | 4215 |
| rs755715664 | snp | A/G | 1.75087e-05 | 0.00295872 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689682 | GTGGGCGCCTGCGGA[A/G]TGCGGACAGCGAGAA | 4215 |
| rs755763179 | in-del | -/AAA | | | cds-indel, downstream-variant-500B, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63695090 | AGTTGTCATTAAAGG[-/AAA]AAAAAAAAAAAAAAA | 4215 |
| rs755773590 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675860 | CTGTTTTGCATAGCT[C/T]TGTGCTTTGGGCTGT | 4215 |
| rs755792729 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677075 | CTACGGAGTTCCTAC[C/T]GTGAGATGGGGTTAT | 4215 |
| rs755799826 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646764 | AAAAAATGTGACTGT[A/C]CTTAATTTCTGAAGT | 4215 |
| rs755843514 | snp | G/T | 4.99106e-05 | 0.00499528 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632634 | GTGAAAGAGCTTTGC[G/T]GGTCTGTATTTAAGT | 4215 |
| rs755857805 | snp | C/T | 3.30136e-05 | 0.00406273 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691751 | TCGGTGAAAGACCAG[C/T]TGAAGGCTTACGGTG | 4215 |
| rs755861555 | in-del | -/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694769 | AGTCGTGACCTGCTA[-/G]GGCCAGAGCCCACTC | 4215 |
| rs755874324 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655764 | CTCCTAGGATTACAG[A/G]TGTGAGCCACTATCC | 4215 |
| rs755876450 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688775 | GAAGCCAGTGATTCC[C/T]CTGTCTTACTCAGAT | 4215 |
| rs755952221 | snp | C/T | 1.64931e-05 | 0.00287163 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691839 | ACCTGCACAGCAACA[C/T]GATTGTTCACCGGGA | 4215 |
| rs755956827 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632367 | CATGGTGGTGCATGC[C/T]TGTGTTCCCAGCTAC | 4215 |
| rs755968583 | snp | G/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691309 | GGCCTGCAGGAGGGG[G/T]GTCACCTTGGATAGG | 4215 |
| rs755976810 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667760 | TGCTATATTTTTATT[C/T]GTATTTTTTTGCTAT | 4215 |
| rs756058538 | in-del | -/A/AA | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670586 | GTGAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 4215 |
| rs756062923 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654244 | CTCTCCTCTTCTCAG[C/T]TCTTGGTAAGCACTT | 4215 |
| rs756069726 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692762 | CTCAAGACAGTTTGC[A/G]CTTGCTCGACATAAC | 4215 |
| rs756088939 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683739 | TGACTTTACTGAAAA[A/G]TGAAAATATGATAAG | 4215 |
| rs756134595 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668792 | ACACGGCCTCTTAGC[A/T]TACCTAGATCCTGGC | 4215 |
| rs756155116 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659044 | CCCGGCCATTTTTTA[A/G]TTTTTTTAGTAGAGA | 4215 |
| rs756203244 | snp | A/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693820 | GCCCTTTGCTGCATG[A/G]CAGGGGGCTGCTGCT | 4215 |
| rs756214321 | snp | C/T | 3.53688e-05 | 0.00420513 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691018 | AGATCCCTGTGAGGC[C/T]ACTAACTAGGGCAAG | 4215 |
| rs756228667 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667715 | CGGGTTATTTATAAT[A/G]TGATGTAAATACTAT | 4215 |
| rs756240701 | in-del | -/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670285 | GTGCTGCAGGTGGGC[-/T]TATAACTAAGAAATG | 4215 |
| rs756295317 | snp | A/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694606 | GCCTAGGCTGCATTG[A/G]AAAGAGCTGAAGGTT | 4215 |
| rs756301178 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672604 | ACCATGCACCCAGGC[A/G]AGAGTGCCTAAGCAG | 4215 |
| rs756320615 | snp | A/T | 1.6654e-05 | 0.00288561 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652642 | CCTCTTGATCTACAT[A/T]ACATGAACAATGAGG | 4215 |
| rs756402054 | in-del | -/GTAGCTGT | 1.68505e-05 | 0.00290258 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646095 | TCTGCCTTCTGATGA[-/GTAGCTGT]GTTCATGTATGCCAA | 4215 |
| rs756420339 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657965 | TGCTTTCCTTCAGGA[A/T]CTTGTCTCGCCTCCT | 4215 |
| rs756476823 | snp | A/C | 1.93493e-05 | 0.00311035 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692443 | TGGGACATGCAGAAC[A/C]CATTCTTCCACCCAG | 4215 |
| rs756493265 | snp | C/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686426 | TGTAGCCTTGTTTGG[C/G]GCTTGCTTTCCAACC | 4215 |
| rs756497233 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671034 | AACAGATTGGAGGGG[C/G/T]CAAGAATGCATGCAA | 4215 |
| rs756518158 | snp | A/G | 1.68142e-05 | 0.00289945 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634684 | AGGATACAAATTATT[A/G]ACCTCAGTTTTTTTG | 4215 |
| rs756583166 | in-del | -/ATG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666219 | GGCACAATGGTACTT[-/ATG]ATAGCTTTTCCCAAT | 4215 |
| rs756606204 | snp | G/T | 1.64909e-05 | 0.00287144 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634778 | AGCTCATGTGCAGGG[G/T]CCAGTGAGAAAAAGA | 4215 |
| rs756693059 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634559 | TGAAGTCAGTGGTTA[G/T]GAAGGCAGAAGCCTA | 4215 |
| rs756731336 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651851 | TCCTGTGACTCTGTA[A/G]TAGAAAATCTTAATT | 4215 |
| rs756731667 | snp | C/G/T | 8.23898e-05 | 0.00641786 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667029 | TACTATCTACCAGCC[C/G/T]CCCGAGCCCAGAAGC | 4215 |
| rs756732722 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651754 | CTCTCCAGAAAATCT[C/T]CAATGTCAATACTAG | 4215 |
| rs756808678 | snp | C/T | 6.59402e-05 | 0.00574158 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690356 | GACGTGGACACGGGA[C/T]GTGAACTTGCTTCCA | 4215 |
| rs756925584 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665233 | TACAGTGGTGCGATC[G/T]CGGCTCACTGCAAGC | 4215 |
| rs756948307 | snp | A/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676997 | GGCACAGTAGAAGGG[A/T]GGAATCCATCTTACG | 4215 |
| rs756997078 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688866 | GTGTCTGTGCACCAC[A/G]AGGACTACAGTGATG | 4215 |
| rs757017615 | snp | C/T | 1.81777e-05 | 0.00301472 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652510 | GCTTTTTAAACCCTA[C/T]GTTTTAAGTATACAA | 4215 |
| rs757072888 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693483 | GCGCCTCTTTCTGCA[G/T]TGGTGGGCAGGACAG | 4215 |
| rs757080337 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641994 | AGAGAGGACAAGAAG[A/G]ATGGCTGGCCGGAAG | 4215 |
| rs757086427 | snp | G/T | 2.01448e-05 | 0.00317364 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689532 | TCTCCTCTGGCCCTT[G/T]CACCCTTTCAGGCAG | 4215 |
| rs757112592 | snp | C/T | 1.65441e-05 | 0.00287607 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692228 | GTTGCAGCCTCTGCC[C/T]TTTCATGCCTCAGGA | 4215 |
| rs757172713 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666732 | TCTCAGCGCTCATAC[A/G]TCATTGAAGCTATAA | 4215 |
| rs757199472 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640925 | CATTCTGCCTCTACC[A/G]CAGTAGTACTGTCTC | 4215 |
| rs757202721 | snp | C/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694634 | GTTGTGGCCTTTGCG[C/G]TCCTGGCCCAGCCTT | 4215 |
| rs757228836 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670853 | GAAGGGGAGGGCAGG[A/G]TGAAGCTGGGGAGGG | 4215 |
| rs757230947 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655533 | GTTTCACTTTGTTGC[A/G]CAGGCCAGAGTGCAG | 4215 |
| rs757293519 | in-del | -/TA | 3.69812e-05 | 0.00429991 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657777 | ATTATTTTCCTTTTC[-/TA]TGTCTTGTATCACAG | 4215 |
| rs757295155 | snp | G/T | 0.000496787 | 0.0157527 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688516 | CTGTTTTTTCTTTTT[G/T]TTTTCTCCAGCCCAT | 4215 |
| rs757301334 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660874 | GTGCTGGGATTACAG[A/G]CATGAGCCACTGCAC | 4215 |
| rs757306885 | snp | C/T | 1.65089e-05 | 0.00287301 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691850 | AACATGATTGTTCAC[C/T]GGGACATTAAGGGTG | 4215 |
| rs757319416 | in-del | -/ATGGCCGCCATCTTCAAG | 1.65192e-05 | 0.00287391 | cds-indel, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693612 | GCAGAGTATGAAGCT[-/ATGGCCGCCATCTTCAAG]ATGGCCGCCATCTTC | 4215 |
| rs757320092 | snp | C/G | 1.64901e-05 | 0.00287137 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691204 | CGCGCTGAGAAGACC[C/G]TGACCATCTTCATGG | 4215 |
| rs757334255 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647891 | AGAATTAGAATTCAC[A/G]GGAAAGAGGAAAGAA | 4215 |
| rs757343056 | snp | C/G | | | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695883 | GGACATGCTGGCTCA[C/G]CATCCTCAGGACCAA | 4215 |
| rs757364517 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631344 | CTTGAGCAGTTTTAC[C/T]TCCTACATTTCATGC | 4215 |
| rs757370145 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643588 | CTGCTCTGTATGCTC[A/G]GTTTTTCTGTAAATG | 4215 |
| rs757430511 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659457 | ATCCTCACCTCTAGA[A/G]CAGTGTTCCTCTAAC | 4215 |
| rs757435080 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681699 | CCTAATAGTTGGCCC[C/T]ATGCCTGCTCCTCTT | 4215 |
| rs757496395 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623810 | GGTAAACTTCAGTGA[A/G]AGGATCGTTTGCAAA | 4215 |
| rs757545149 | in-del | -/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663208 | ATGAACAGTGTAAAA[-/G]TTTACAATGCTTGGC | 4215 |
| rs757547023 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646684 | CTCTTCTGTCCTTTT[A/C]TCCATTGTCAGTATT | 4215 |
| rs757620907 | snp | C/G | 1.70825e-05 | 0.00292249 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690240 | ATGTACACAAAGTAA[C/G]TCTTTCCTTCTGCTC | 4215 |
| rs757622671 | snp | A/G | 0.000101249 | 0.00711436 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646017 | TTCTCTAACCTGTCT[A/G]TCATTCTTTTTGGCA | 4215 |
| rs757626698 | snp | A/G | 1.65228e-05 | 0.00287422 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693619 | TATGAAGCTATGGCC[A/G]CCATCTTCAAGATTG | 4215 |
| rs757627239 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679042 | TCAAAAAAAAGAGTC[A/G]GTGTCAGTTTCTTAA | 4215 |
| rs757667016 | snp | C/T | 3.29864e-05 | 0.00406105 | intron-variant, splice-donor-variant | MAP3K3 | GRCh38.p7 | 17:63634803 | AAAAGAAATTTTTGG[C/T]AAGGATCCAGATTAC | 4215 |
| rs757695070 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621756 | AGGCCAGACCCTCCC[C/T]ACTCGTTACACGCCC | 4215 |
| rs757697531 | in-del | -/T | 0.000152917 | 0.00874271 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646011 | GAGAATTCTCTAACC[-/T]TGTCTATCATTCTTT | 4215 |
| rs757763563 | snp | G/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686502 | TAGACTGAGGGCTCT[G/T]CCAAGACAGGGATTG | 4215 |
| rs757773410 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688953 | TGGGGAGGGTGGGTT[C/T]GTCCATGCAGTGCCT | 4215 |
| rs757799496 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636189 | AGCAAGACTTGAGAC[A/G]TCCTTTTCCCTAAGT | 4215 |
| rs757829589 | snp | G/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672754 | AGGAAAGGAAATTAG[G/T]AGTGTGGGGAGAAGG | 4215 |
| rs757854943 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638158 | AGATTGCTTTATAAT[C/T]GTCTCTTCCACTGAT | 4215 |
| rs757878659 | snp | C/T | 0.000181304 | 0.00951941 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632796 | CACAGGTCACTCAAA[C/T]AGGCAGGTGTGTGTG | 4215 |
| rs757888966 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637884 | TTCATGAGTGGGTGC[C/T]TCAGAACAGAAAAGC | 4215 |
| rs757921740 | snp | C/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686776 | TGCCTGCAGTACTTT[C/G]TTTTCTTCTCATTGT | 4215 |
| rs757927190 | snp | C/T | 1.65422e-05 | 0.0028759 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692291 | AAAGCTGGGGGACTT[C/T]GGGGCCAGCAAACGC | 4215 |
| rs757944773 | snp | C/G/T | 7.21024e-05 | 0.00600389 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681762 | CCTCCTTTATGTGCT[C/G/T]TAGGCTCCCAGAACC | 4215 |
| rs758009711 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689389 | GGTGGGAGTGCGGAC[A/G]GGATGGGCTGGAGCT | 4215 |
| rs758013217 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666169 | GGGTGCTGGGAGGAT[G/T]GCTGACCCTCCTCTC | 4215 |
| rs758047144 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652848 | GATTACTCAGCCATC[A/T]CAGCCATCTCCATTC | 4215 |
| rs758121860 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678466 | AGTGAGATGTTGAGA[C/T]AGGAAATCCAGCAAA | 4215 |
| rs758129357 | snp | A/C | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621674 | GCCCGGGGCAAGAGC[A/C]GCGTCGGGACCGGAG | 4215 |
| rs758223758 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633508 | TTAAAATGTCACCTA[G/T]TATATTCTGAAGGCA | 4215 |
| rs758240670 | snp | A/C | 1.73219e-05 | 0.0029429 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689665 | GCAATACCTGGACCC[A/C]CGTGGGCGCCTGCGG | 4215 |
| rs758322494 | snp | C/G/T | 3.42796e-05 | 0.00413991 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657789 | TTCTATGTCTTGTAT[C/G/T]ACAGCTCTCCATCCT | 4215 |
| rs758359143 | snp | A/G | 1.86339e-05 | 0.00305231 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689554 | TTCAGGCAGAAGAAC[A/G]TTTCCCCGAATACGG | 4215 |
| rs758373687 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642247 | ACAAAAGTTTAATTC[C/T]CTTTCTGAATAAATT | 4215 |
| rs758436288 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684083 | GGGAGGATCACTTGA[A/G]CCCAGGCTGCAGTGA | 4215 |
| rs758445073 | snp | C/T | 1.65111e-05 | 0.0028732 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688748 | CTTAAGTGGCTCACA[C/T]TGACCTACCCAGAAG | 4215 |
| rs758455809 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644126 | CAATGCTTGGTTTGT[A/G]GTAAATGCTCAATAA | 4215 |
| rs758462712 | snp | C/T | 0.000133976 | 0.00818354 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646027 | TGTCTATCATTCTTT[C/T]TGGCAGAGTGACGTC | 4215 |
| rs758477792 | snp | C/T | | | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695651 | ACACTCTTCCTGGCC[C/T]GCACCCCCATCCCCA | 4215 |
| rs758573394 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669124 | GCTGAGCCTGTGAGC[A/G]TTTCCATAGAGCCAA | 4215 |
| rs758574814 | snp | C/T | 1.65296e-05 | 0.00287481 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688523 | TTCTTTTTGTTTTCT[C/T]CAGCCCATCCTTCCG | 4215 |
| rs758582934 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648006 | CCCCTGACTGTCCTC[C/T]CTTTTGGCCCCAGGA | 4215 |
| rs758672983 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650187 | ATTCTTCTGTGAATT[A/G]TCTAATCTTTTGCCT | 4215 |
| rs758673041 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632516 | AAAGAATCCATTAAA[A/G]TTCAAATTGCCATAG | 4215 |
| rs758701034 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661468 | GACCACCAACTTTTA[C/G]CTTATGCATCTAACT | 4215 |
| rs758707269 | snp | G/T | 0.000101036 | 0.00710687 | intron-variant, nc-transcript-variant, splice-acceptor-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690992 | TTTTCTCCAACTGCA[G/T]TTCCCAAGGCAGATC | 4215 |
| rs758723781 | snp | A/G | | | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696007 | TTCCTGGCAGCCCCA[A/G]GCTTGCTGTGGGAAG | 4215 |
| rs758777290 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646905 | TTTTTTCCACTCTTT[A/G]CCTTTCTTTCCCATT | 4215 |
| rs758806722 | snp | C/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672018 | CCAGGTTTGGTGGCT[C/G]ACATCTGTAATCCCA | 4215 |
| rs758870331 | snp | A/G | 1.70563e-05 | 0.00292025 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646116 | GTGTTCATGTATGCC[A/G]AAGTTCTCAGATAGC | 4215 |
| rs758893179 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639105 | AGTGAGGACTACATG[A/G]AAAAAAGAAAGTATG | 4215 |
| rs758926879 | snp | A/C | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63622044 | CCAAGAGAGGGAGAC[A/C]GCACCAGAGAGGGAT | 4215 |
| rs759018530 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635742 | ATTGTAGTTTTTGTT[A/T]GCCTAGGCCTGAGAT | 4215 |
| rs759020124 | snp | A/G | 3.35295e-05 | 0.00409434 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693786 | GTACTGAGCTCTCAC[A/G]GCCACACAGCTGCCG | 4215 |
| rs759035815 | snp | A/G | 0.00258946 | 0.035889 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645983 | CTTGGCAATGGCAGG[A/G]GTGACACATTCCAGA | 4215 |
| rs759041035 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656222 | GCAACAGAGGGAGAT[A/G]CTGTCTCAAAAAAAA | 4215 |
| rs759061216 | snp | C/G | 1.65241e-05 | 0.00287433 | missense | MAP3K3 | GRCh38.p7 | 17:63693563 | GGAGCCTGGGCTGCA[C/G]TGTGGTGGAGATGCT | 4215 |
| rs759095415 | snp | C/G | 4.94572e-05 | 0.00497254 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688582 | TTCCCTGACAACAGA[C/G]AGGAATACTCAGGTG | 4215 |
| rs759110846 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692139 | TGTCTAATTCAGTGG[C/T]AGCCCTGCCCTCTCC | 4215 |
| rs759162560 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694135 | GGGGCACAAGACTGA[C/T]GCCAGGGTATGAAGA | 4215 |
| rs759188734 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684744 | TGATCCTTCCCTCTC[A/G]GCTCCCAAAGTGCTA | 4215 |
| rs759198719 | snp | C/G | 1.6806e-05 | 0.00289875 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688476 | CTGGACGCCCTGCTT[C/G]GTTGCTGTGGAAGTG | 4215 |
| rs759209044 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633810 | ATGTTTGATGAAAAT[G/T]TGTGTATGACATTCT | 4215 |
| rs759233191 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655238 | AAACCATCAGATCTC[A/G]TGAGAACTCACTCAC | 4215 |
| rs759238510 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649150 | CTTTTAAGACAGGGT[C/T]TCTGGGCCAGGTACA | 4215 |
| rs759254523 | snp | A/G | 1.64955e-05 | 0.00287184 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634764 | CCACAGTAACAACAA[A/G]CTCATGTGCAGGGGC | 4215 |
| rs759283415 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669862 | ATCCCAGCACTTTAG[A/G]AGGCCGAGTTGGGTG | 4215 |
| rs759352927 | snp | C/G | 1.64852e-05 | 0.00287094 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690315 | TCCTGGGCCAGGGTG[C/G]CTTCGGCAGGGTCTA | 4215 |
| rs759390854 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632234 | GGCCCACACCTGTAT[A/G]TAATCTTAGCACTTT | 4215 |
| rs759432729 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662088 | AGCCTGAGCCACAGA[A/G]CGAGACTCCATCTCA | 4215 |
| rs759442484 | snp | A/T | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667012 | TCCGCAGGGGATATA[A/T]ATACTATCTACCAGC | 4215 |
| rs759454901 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625568 | TCAGAATTATTGTGA[C/T]TTACAGACACCTTGT | 4215 |
| rs759502592 | snp | C/T | 0.00021721 | 0.0104191 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689517 | TGGGGTGTGACTTGC[C/T]CTCCTCTGGCCCTTG | 4215 |
| rs759531607 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669387 | GGGACTCTCAGCTGC[A/G]CTCAGACTCTTTTGG | 4215 |
| rs759545233 | snp | C/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672198 | TGAGGCAGGAGAATT[C/G]TTTGAACCCGGGAGG | 4215 |
| rs759553694 | in-del | -/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692986 | CTGGATTAAGGGTCC[-/T]TACAGAAGGGTCTCA | 4215 |
| rs759589907 | in-del | -/ATG | | | intron-variant, downstream-variant-500B, cds-indel | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696613 | GTTCCCGGAGCTTTC[-/ATG]ATATTTGGTAGGGTC | 4215 |
| rs759611885 | in-del | -/GTT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650696 | AGAGAGAGAGAGAGA[-/GTT]TTTTTTTTTTTTAGA | 4215 |
| rs759615626 | snp | C/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696800 | AAGTTGGCCTGCCCT[C/G]AGAGGCTCTGAGGCG | 4215 |
| rs759623089 | snp | G/T | 1.65258e-05 | 0.00287448 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632848 | ATTTGTTGGGGAGGG[G/T]TTTTCAAATGGGAAA | 4215 |
| rs759627020 | snp | A/G | 1.65603e-05 | 0.00287747 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692211 | ATGCAAGAGGGTCCA[A/G]GGTTGCAGCCTCTGC | 4215 |
| rs759627537 | snp | A/C | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688283 | GAGAGGGCTGTGCAG[A/C]CAGGCTGGAGTTGGG | 4215 |
| rs759718736 | snp | C/T | 3.44525e-05 | 0.00415031 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689629 | CCTGAGCACAAATGG[C/T]GAGAACATGGGTCTG | 4215 |
| rs759752747 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651571 | AACTCCCATGGACCT[A/G]TCACCCAGCTTCAAC | 4215 |
| rs759784587 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665767 | TTGGTTCTGACTTCC[C/T]GTTAGAGCAAGACAG | 4215 |
| rs759819596 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686200 | GAACACTTTTGATCA[C/T]GTCTGTCTGGGCTTA | 4215 |
| rs759850043 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654450 | GATATACCACATTTT[A/G]TGTATCTGTTCATCT | 4215 |
| rs759896282 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644029 | AATCTTATTGTAACT[C/T]AGTTATTTTCTGTAA | 4215 |
| rs759920304 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628768 | TTCTAATGTGTAATA[C/T]AAGATAAGTATTCAG | 4215 |
| rs759921748 | in-del | -/TTTGGGAGGGT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645430 | CCCCAGTGGGGTAGC[-/TTTGGGAGGGT]TTTGGGAAATCAATG | 4215 |
| rs759929676 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693264 | CCTCTAAGTTTGTGG[G/T]CATTTGTTAAGAGCA | 4215 |
| rs759979177 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657150 | TTTTCTGCTTGTTCT[A/G]TTAATGTCAGCACAA | 4215 |
| rs759988158 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679132 | CTGGCCAGGCATGGG[A/G]GCCCATGCCTTTAAT | 4215 |
| rs760060741 | snp | A/G | 1.65551e-05 | 0.00287702 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657880 | GAAAAGCCTTAGGAT[A/G]TTGCTGTTGTCCCAG | 4215 |
| rs760087586 | in-del | -/C | 1.65941e-05 | 0.00288041 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691282 | CAAAAGAGGGCCTGA[-/C]CTGGGGGCTGGGGCC | 4215 |
| rs760173121 | snp | C/T | 1.65767e-05 | 0.00287891 | synonymous-codon, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693747 | AGCTGAGGAGCTGCT[C/T]ACACACCACTTTGCA | 4215 |
| rs760247312 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678087 | AATTGCCTTGGCTGA[A/G]CTGTATGAGAGTCAC | 4215 |
| rs760318870 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632304 | GGAGACCAGCCTGGG[A/C]AACATGGGGAGACCC | 4215 |
| rs760333977 | snp | A/G | 9.88566e-05 | 0.00702983 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688813 | CTCAGCTTTATGACA[A/G]AGGGGTCAAAGGTGG | 4215 |
| rs760379130 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635004 | TATCAGTGCTGTCCA[A/G]TAAACCTTCTGTGAT | 4215 |
| rs760423316 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657386 | GAATCTTTATGAATT[G/T]AATTGAATATGTATG | 4215 |
| rs760423930 | in-del | -/GTC | 1.77647e-05 | 0.00298027 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622770 | CCACCATGGGTAAGT[-/GTC]GCCACCGCCCCGGCC | 4215 |
| rs760427972 | snp | A/G | 1.68536e-05 | 0.00290285 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646093 | AGTCTGCCTTCTGAT[A/G]AGTAGCTGTGTTCAT | 4215 |
| rs760447616 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693352 | TCTTTTTCCTTATTT[C/G]AAGAAGTACCCAGGT | 4215 |
| rs760456916 | snp | G/T | 1.74157e-05 | 0.00295085 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681842 | CATTGCCCGGCAGGG[G/T]TCCTACACCAGCATC | 4215 |
| rs760498731 | snp | C/T | 3.61906e-05 | 0.0042537 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681718 | CCTGCTCCTCTTGGG[C/T]CACACACCCTGGGCT | 4215 |
| rs760586639 | snp | A/G | 6.59196e-05 | 0.00574068 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632741 | TCCAGATGAACCGAC[A/G]TCACCGGATGCCTGG | 4215 |
| rs760651201 | snp | A/G/T | 5.44819e-05 | 0.00521905 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657778 | TTATTTTCCTTTTCT[A/G/T]TGTCTTGTATCACAG | 4215 |
| rs760661346 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623642 | GTTGAATTATATTCC[A/G]TATCCTTTTTGGTAG | 4215 |
| rs760754907 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685032 | TTTGTTCTGGTATCA[A/G]CTGTGCACTAACTAG | 4215 |
| rs760793020 | in-del | -/GCA | 1.65559e-05 | 0.00287709 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692216 | AGAGGGTCCAGGGTT[-/GCA]GCCTCTGCCCTTTCA | 4215 |
| rs760860103 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688661 | CAGGTGGCTCTGCTT[C/T]GACTTTTCTGAGTCA | 4215 |
| rs760879872 | snp | A/G | 1.6966e-05 | 0.00291251 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657924 | TAAGTAGCCCTTGTC[A/G]TGGTCTGGCAGCTGA | 4215 |
| rs760915893 | snp | A/G | 1.66879e-05 | 0.00288855 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691705 | GCCCTCCCCTGAGGG[A/G]ACTCCTCTGACTTCT | 4215 |
| rs760927080 | in-del | -/AC | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692482 | GGCCCCCCATTAGAA[-/AC]ACACCCTGGGGACTT | 4215 |
| rs760973547 | snp | G/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670341 | TAACCCCAGCACTTG[G/T]TGAGGCCGAGGTGAG | 4215 |
| rs761030867 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644939 | CTTTCTTTTCCTCTA[C/T]ACCTGTTCTTCTGTA | 4215 |
| rs761104061 | snp | C/T | 4.94197e-05 | 0.00497066 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666979 | GTGTCCAGACAGGTG[C/T]GGATCAAGGCTTCCC | 4215 |
| rs761115799 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628903 | AATAATAGCCAGCAT[G/T]TTTTTAGCATTACTG | 4215 |
| rs761117004 | snp | A/T | 3.31142e-05 | 0.00406891 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652570 | AGAATTATAGCGTTC[A/T]GCCGGCCTGTGAAAT | 4215 |
| rs761154998 | snp | A/C/G | 3.29702e-05 | 0.00406008 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691781 | GCTCTGACAGAGAGC[A/C/G]TGACCCGAAAGTACA | 4215 |
| rs761176612 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688589 | ACAACAGACAGGAAT[A/G]CTCAGGTGAGTTCCA | 4215 |
| rs761201602 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629849 | AATGCCAGGAATTGG[C/T]TAGCTTCCTGGAAAC | 4215 |
| rs761284169 | snp | A/G | 1.80951e-05 | 0.00300786 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691064 | GCGGGCAGAACTAGG[A/G]CCCTGAGAGCTGAGG | 4215 |
| rs761320750 | in-del | -/TTC | 1.65255e-05 | 0.00287445 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688887 | TACAGTGATGGTGAG[-/TTC]TTCTTCACCTGCTCC | 4215 |
| rs761353185 | snp | C/G | 3.36559e-05 | 0.00410205 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690972 | GACAGTTAAGAGAGT[C/G]CCCCTTTTCTCCAAC | 4215 |
| rs761375044 | snp | C/T | 1.80837e-05 | 0.00300691 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681737 | ACACCCTGGGCTCTG[C/T]TGTTGAAAGCCTCCT | 4215 |
| rs761423168 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635688 | TAATCATTTAACATC[A/G]GATTTTATAATTCAC | 4215 |
| rs761430030 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694264 | AAAGGCCAGCACTCG[C/T]TAGCAGTGGCAGGCA | 4215 |
| rs761488895 | snp | G/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621417 | AGGTAGGAAATAGAT[G/T]ATCTCTGGGGTGGGA | 4215 |
| rs761505324 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658867 | AGCCTCTCGAGTAGC[G/T]GGGATTATAGGTGCC | 4215 |
| rs761520235 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679578 | GCCTCAACCTCCCAG[A/G]CTCAAGCAGTCCTCC | 4215 |
| rs761571763 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645060 | TGTCATTTTAACATT[C/T]CTACTTCCTCTTATT | 4215 |
| rs761628587 | in-del | -/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676344 | TTCAGTGCAGCTGAT[-/G]AAGGAGGGGACAGGT | 4215 |
| rs761666662 | in-del | -/AG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650660 | CTCTGTCTCTTATAG[-/AG]AGAGAGAGAGAGAGA | 4215 |
| rs761675837 | snp | C/T | 3.29924e-05 | 0.00406142 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681890 | CATCCCAGAGACCAG[C/T]GAGCAGTGCGTGAGT | 4215 |
| rs761683779 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635345 | AGATTTCTGTTTTAG[A/G]AAGAATGTGAAGATG | 4215 |
| rs761701924 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657591 | GCACAACTATGTAAA[A/G]GTACTACAAATTTTT | 4215 |
| rs761703582 | snp | A/C | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673607 | TAAGCCATGTAACCA[A/C]GCCTCAACTAAAGGA | 4215 |
| rs761709890 | snp | A/G | 3.32773e-05 | 0.00407892 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692346 | ACGGGCATGCGCTCC[A/G]TCACTGGCACACCCT | 4215 |
| rs761767735 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636847 | AAGACTGCGTTGGTG[A/G]TCAAGTCCTCCATCC | 4215 |
| rs761895955 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671546 | GGAGTGAGCCACCAC[A/G]CCTGGCCCTCAAAAT | 4215 |
| rs761905810 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691960 | CCATTCTGAACTTTC[C/T]GAAAAGTGGGACCCC | 4215 |
| rs761989024 | snp | C/T | 9.50525e-05 | 0.00689327 | utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622740 | CACGGACCTTAGCCA[C/T]CGCCGCCGCCATCGC | 4215 |
| rs761999490 | snp | G/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676389 | GGATATTTTATCCCA[G/T]GGAAGTCTCACCCCA | 4215 |
| rs762066955 | snp | A/C/T | 6.59135e-05 | 0.00574047 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688832 | GGTCAAAGGTGGAAC[A/C/T]TACCCCCGGCGCTAC | 4215 |
| rs762078603 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661148 | GCCTCCCAGATTCAA[A/G]TGATTCTCCTGCCTC | 4215 |
| rs762113008 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667041 | GCCCCCCGAGCCCAG[A/G]AGCAGGCACCTCTCT | 4215 |
| rs762185565 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667126 | TTAAAAAAGCAACAA[G/T]TATTTGTTAATTAAA | 4215 |
| rs762235370 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631844 | AAACTTGTAAAGAGT[G/T]GTGGGGGTTGCTGGT | 4215 |
| rs762237596 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654871 | TGAAACGCCGTCTCT[A/G]CTGCTGATATAAAAA | 4215 |
| rs762267894 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638955 | CGCTTGTACTTGGGA[A/G]GCGGAGGTTGTAGTG | 4215 |
| rs762270961 | snp | A/C | 1.64833e-05 | 0.00287078 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691789 | AGAGAGCGTGACCCG[A/C]AAGTACACGCGGCAG | 4215 |
| rs762277891 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653818 | CCATTCAGTGGTTTT[C/T]AGTATGCTGATAGAG | 4215 |
| rs762278034 | in-del | -/CTT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650637 | TATGGTTAGGAAGAC[-/CTT]CTCTCTCTCTGTCTC | 4215 |
| rs762349103 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691184 | ACTATGGCTGTCTGC[A/G]GGACCGCGCTGAGAA | 4215 |
| rs762427865 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649173 | CAGGTACAGAGGCTC[A/T]CGCCTGTAATCCCAG | 4215 |
| rs762439194 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685619 | GGTGGTTTGGAGGGT[A/G]ATGCATAGGCATTTT | 4215 |
| rs762499560 | snp | A/G | 3.6205e-05 | 0.00425455 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681908 | GCAGTGCGTGAGTAT[A/G]GGGGGGCTGGGATAT | 4215 |
| rs762529455 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633309 | TTGTGTAAGCATTTC[A/G]TCTGTTATGGGGACA | 4215 |
| rs762559098 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681211 | GATCCTGGCCAGACC[A/G]TCACGAAGGCCTTTT | 4215 |
| rs762578136 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694347 | CCTTTACCAAAGATG[A/C]ATGAAGCAAATGTCA | 4215 |
| rs762633338 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630235 | TTAATATATAAACCT[A/G]TACATATTATATATA | 4215 |
| rs762648029 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667334 | TTGCCTCAGACATCT[A/G]CTTGAAGACTTCCAG | 4215 |
| rs762726420 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683010 | TTGGCTTAGTGAACT[C/T]ACCAAGCATGAGATC | 4215 |
| rs762730732 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674062 | TCCAGCTTAGGCAAC[A/G]GAGTGAGACTCTGTC | 4215 |
| rs762747364 | snp | A/T | 1.68522e-05 | 0.00290272 | missense, intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692385 | AGCCCTGAGGTGATC[A/T]GCGGCGAGGGCTATG | 4215 |
| rs762781489 | snp | C/T | 1.65395e-05 | 0.00287567 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693544 | ACGGGGTTCTCTCTT[C/T]CCAGGAGCCTGGGCT | 4215 |
| rs762806132 | snp | C/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621587 | CAGCCTCGGGTGTCT[C/G]AGGTACCTAGACCAG | 4215 |
| rs762832722 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645424 | CTTTACCCCCAGTGG[C/G]GTAGCTTTGGGAGGG | 4215 |
| rs762880052 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638810 | CCAACACTTTGGGAG[G/T]CCGAGGCAGGCGGAT | 4215 |
| rs762964379 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685214 | TAGTACCATCTCCAG[C/T]GCCAGGCTCCAGTGT | 4215 |
| rs762979122 | snp | A/T | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681484 | TAAAAGCTAGTCTGA[A/T]TGCCAGCTAAAATGG | 4215 |
| rs762993883 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691819 | GATCCTGGAGGGCAT[A/G]TCCTACCTGCACAGC | 4215 |
| rs763042591 | snp | C/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677721 | CTGCATGAAACATGC[C/G]ACTGTGGATGTGGCT | 4215 |
| rs763081777 | snp | A/G | 3.29587e-05 | 0.00405934 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688840 | GTGGAACCTACCCCC[A/G]GCGCTACCACGTGTC | 4215 |
| rs763128893 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645252 | AGGTTGCGGTGAGCC[A/G]ATATTGTGCTACTGC | 4215 |
| rs763130264 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664659 | TTAGCCACAGCTAAC[A/T]TCTACCCAGAGTCCT | 4215 |
| rs763151406 | snp | A/G | 1.65633e-05 | 0.00287774 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692195 | GGGAGGATGGGAGAA[A/G]ATGCAAGAGGGTCCA | 4215 |
| rs763207767 | snp | G/T | 9.53516e-05 | 0.00690411 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622785 | GTCGCCACCGCCCCG[G/T]CCTGTGCCCGCGCTG | 4215 |
| rs763348565 | snp | A/C | 1.91716e-05 | 0.00309603 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652705 | GGGGCAGATGCCTAC[A/C]TTTTTTCTCTCTGTT | 4215 |
| rs763357768 | in-del | -/TG | 1.68559e-05 | 0.00290304 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634659 | ATGTTGTCAAACTTA[-/TG]TTGCACGAAGGATAC | 4215 |
| rs763359325 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641477 | CGAACTCCTGACCTC[A/G]TGATCTGCCCTCCTT | 4215 |
| rs763385883 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676718 | AGACACACCACAGAG[C/T]GTCCTCCCTCTTCTG | 4215 |
| rs763395208 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625891 | AGCCTGGGCAACATG[A/G]TGAAACCCTGTCTCT | 4215 |
| rs763422381 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693168 | CCAGCCCTGCCGCCA[C/G]CTTGACTTTAGCCCT | 4215 |
| rs763455679 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628666 | GGCCCTGCCAATTCT[A/G]TCTTTTTTTTCATAC | 4215 |
| rs763486928 | in-del | -/C | 1.7947e-05 | 0.00299553 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622816 | CTTCGCGACGCCCCG[-/C]CCCAGGCTGAGGGAG | 4215 |
| rs763487369 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656153 | GAGGATCACTTTAGC[C/T]CAGGAGGCGGAGGTT | 4215 |
| rs763526019 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690351 | GCTATGACGTGGACA[C/T]GGGACGTGAACTTGC | 4215 |
| rs763548643 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694096 | TCCTGACACTGCAAT[A/T]GGCACCGAAGCCCAG | 4215 |
| rs763615408 | snp | A/G | 3.38232e-05 | 0.00411223 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690457 | TCCCTCCTTTCAACA[A/G]AAATGCCTGTCTTAC | 4215 |
| rs763617586 | snp | A/C/T | 8.23942e-05 | 0.00641806 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667028 | ATACTATCTACCAGC[A/C/T]CCCCGAGCCCAGAAG | 4215 |
| rs763626238 | in-del | -/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693944 | GCTCAGAGCCGGGGT[-/G]GGGGTGGCTGCAGCC | 4215 |
| rs763634683 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621767 | TCCCCACTCGTTACA[C/T]GCCCTGTGCTGGGCA | 4215 |
| rs763706996 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679529 | ACTCTATCACCTATG[C/T]TGGAGTGCAGTGGTC | 4215 |
| rs763735262 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670331 | CTCACGCCTGTAACC[C/T]CAGCACTTGGTGAGG | 4215 |
| rs763744054 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693397 | GGTCCATGAAGCCCA[C/T]GTGGACAGACATCCA | 4215 |
| rs763772663 | in-del | -/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631648 | GAATTGGACTGGTTT[-/G]TGTTCTGGGTTTTGG | 4215 |
| rs763790876 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641753 | ATTGAGGAATCATCT[A/G]TTTAGAGGCCCACTG | 4215 |
| rs763858218 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636790 | GAGGCAGCCCGGCTG[A/T]GGGAGAAGTGGCTGA | 4215 |
| rs763892428 | snp | C/T | 0.000118017 | 0.00768079 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646096 | CTGCCTTCTGATGAG[C/T]AGCTGTGTTCATGTA | 4215 |
| rs763919601 | snp | C/G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634143 | CATATGTTATTCAGT[C/G/T]TGACTGTGTGAGTTC | 4215 |
| rs763933046 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670411 | AACACAGTAAAACCC[C/T]GTCACTAATAAAAAT | 4215 |
| rs763963513 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620482 | GTATTAGCATAATAA[C/T]CTTAGAGTTATTGGA | 4215 |
| rs763990174 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656300 | GCTTGATTTTGTGTT[C/T]ACCATACGTGTATAA | 4215 |
| rs764061073 | snp | C/T | 1.80948e-05 | 0.00300784 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681719 | CTGCTCCTCTTGGGC[C/T]ACACACCCTGGGCTC | 4215 |
| rs764072557 | snp | C/T | 1.69666e-05 | 0.00291256 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657925 | AAGTAGCCCTTGTCA[C/T]GGTCTGGCAGCTGAA | 4215 |
| rs764104007 | snp | A/C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659197 | ATTTTTCTATGTTGT[A/C/G]ATTATAATTTGTAAG | 4215 |
| rs764104044 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675197 | ATTCTACCCACTACT[A/G]TGTTCTACAGAGTGT | 4215 |
| rs764123528 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668980 | TTTACTGAGCATCAA[A/G]TAGAGAGAGATATCT | 4215 |
| rs764162783 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635078 | GCCACTAGCTACATG[C/T]GGCTGTTGAGCAACT | 4215 |
| rs764190286 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660979 | TAGTCTTACCTCTCC[C/T]ACCTCACTTTGGCCA | 4215 |
| rs764296538 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673971 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGTG | 4215 |
| rs764315881 | in-del | -/C | 1.65776e-05 | 0.00287898 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693507 | AGGACAGCTGGGAGT[-/C]CAGGGCTGGCTGAGG | 4215 |
| rs764375472 | snp | A/G | 4.95364e-05 | 0.00497652 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690291 | CCATCAACTGGCGCC[A/G]GGGAAAGCTCCTGGG | 4215 |
| rs764418852 | snp | A/C | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688765 | GACCTACCCAGAAGC[A/C]AGTGATTCCCCTGTC | 4215 |
| rs764447042 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623681 | ATGACTACTGGACTA[A/G]ACTAAGAAATAACAT | 4215 |
| rs764458986 | snp | C/T | 3.3024e-05 | 0.00406336 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688616 | TCCACAGAGCCTGGG[C/T]GGGTAATGCAGGGTG | 4215 |
| rs764467307 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626601 | TGAGATTTAGCAAAG[G/T]TTCAACCATTTCTTG | 4215 |
| rs764495536 | snp | A/G | | | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652604 | AAGATGTGGAGCACA[A/G]GGTGACAACAGTATT | 4215 |
| rs764558105 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629880 | AGAATTTGTCAACCT[C/G]ATAAACCAGCTCTTA | 4215 |
| rs764602506 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666085 | TTTTAAGCTTTCTCA[G/T]TGCAAAGGCCCCCCT | 4215 |
| rs764688761 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636011 | AGCCTTTCACTATGA[G/T]AATGGCAGTGCTGGC | 4215 |
| rs764696055 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652805 | TAATTCCAACAACTG[G/T]GGGATCTCTGTTTTT | 4215 |
| rs764725736 | snp | A/T | 5.00271e-05 | 0.0050011 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691708 | CTCCCCTGAGGGGAC[A/T]CCTCTGACTTCTTGT | 4215 |
| rs764750328 | snp | A/G | 1.76708e-05 | 0.00297239 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691070 | AGAACTAGGGCCCTG[A/G]GAGCTGAGGCGACCA | 4215 |
| rs764753984 | snp | A/G | 1.79162e-05 | 0.00299295 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681893 | CCCAGAGACCAGCGA[A/G]CAGTGCGTGAGTATA | 4215 |
| rs764760347 | snp | A/C | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632774 | ATGAGACCATGAAGA[A/C]CAAAGACACAGGTCA | 4215 |
| rs764765927 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652036 | ATTTTTTTCTTTCAA[A/C]TTTTATTTAAGTTCT | 4215 |
| rs764861616 | snp | C/G | 0.000196252 | 0.0099039 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690976 | GTTAAGAGAGTCCCC[C/G]TTTTCTCCAACTGCA | 4215 |
| rs764867822 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630166 | CTTGTATTGATCCCA[A/G]TTTATTATTACAGTT | 4215 |
| rs764888644 | in-del | -/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620526 | ATGACGTGCCTGTTA[-/T]ATTGATAAATACTAA | 4215 |
| rs764900004 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690822 | CTTTCAACGTCGCTT[A/G]TACTTCAAGTTCTGT | 4215 |
| rs764923689 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629025 | AGATGAGGAAATTGA[A/G]GTTTGGAGAGAATAA | 4215 |
| rs764955159 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694235 | GGCTGGATGAGCTCC[A/C]ACAAGCCTGAGGGAA | 4215 |
| rs764965349 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645135 | CAAATATTATTAAGC[A/T]CAAATATTATATGCC | 4215 |
| rs765053642 | snp | C/T | 4.99588e-05 | 0.00499769 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692354 | GCGCTCCGTCACTGG[C/T]ACACCCTACTGGATG | 4215 |
| rs765063571 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657616 | ATTTTTGGATTGTAC[A/G]TTTAGAGAAAAAAAT | 4215 |
| rs765125674 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620643 | TGGGAATATGGCAGG[C/T]TTAAGCTTGTTGGAA | 4215 |
| rs765141594 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632866 | TTCAAATGGGAAATA[C/T]ACGAAAAGCCAAGGA | 4215 |
| rs765143147 | snp | A/C | 3.46164e-05 | 0.00416017 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689662 | TGTGCAATACCTGGA[A/C]CCCCGTGGGCGCCTG | 4215 |
| rs765159612 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643609 | TCTGTAAATGTAAAA[C/T]TCTTCTAAAAATAAA | 4215 |
| rs765215586 | snp | A/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621477 | TTCAATTTTCCTACA[A/G]AAAGCTCGTGTTGCT | 4215 |
| rs765241814 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662792 | CCTCCCTAGTAGCTG[A/G]GATTACAGGCGTGCG | 4215 |
| rs765257077 | in-del | -/TAAAAA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661807 | TCTTCTGGCCCCTGT[-/TAAAAA]TAAACACTGGGCCGG | 4215 |
| rs765258904 | snp | A/C/G | 4.95481e-05 | 0.00497715 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688745 | GGGCTTAAGTGGCTC[A/C/G]CATTGACCTACCCAG | 4215 |
| rs765319295 | snp | A/C | 1.65414e-05 | 0.00287583 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692232 | CAGCCTCTGCCCTTT[A/C]ATGCCTCAGGAGCCA | 4215 |
| rs765335754 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649801 | ATGCAGTTCTAGATG[A/G]TGAAGGCTTTTATGC | 4215 |
| rs765402857 | snp | C/T | 9.22211e-05 | 0.00678985 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622778 | GGTAAGTGTCGCCAC[C/T]GCCCCGGCCTGTGCC | 4215 |
| rs765426489 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678608 | TTGGAGGGAGGCTGG[A/G]GTGATGTGTCCAAGA | 4215 |
| rs765457956 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654908 | GGGCATGGTGGTGCA[A/C]ACCTGTAGTCCCAGC | 4215 |
| rs765459443 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683870 | TTCCAACAAAAATTA[C/T]GTCAGTCCGGTCGCA | 4215 |
| rs765476339 | snp | A/G | 1.6713e-05 | 0.00289072 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690426 | AGGTACACTTAACCC[A/G]TGGTCTGACTTCAGT | 4215 |
| rs765526233 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625704 | ATTGAAATTTGAATC[A/C]CAGTTTAATAAATCA | 4215 |
| rs765568700 | snp | A/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675409 | AGCCCTAGAACTCCC[A/T]GCGGAGACAACTTCC | 4215 |
| rs765592336 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654519 | TAAATAGTGCTGCTA[C/T]GAGCATTTGTTTACA | 4215 |
| rs765617563 | snp | A/T | 1.69198e-05 | 0.00290854 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646104 | TGATGAGTAGCTGTG[A/T]TCATGTATGCCAAAG | 4215 |
| rs765635355 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638990 | GAGATCACTGCACTC[C/G]AGCCTGGGCGACAGA | 4215 |
| rs765721420 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640235 | TAGCGCACAGTGATT[A/G]TGCCTGTGAATAGCT | 4215 |
| rs765789809 | snp | A/G | 5.05131e-05 | 0.00502534 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634674 | TGTTGCACGAAGGAT[A/G]CAAATTATTAACCTC | 4215 |
| rs765873873 | in-del | -/AA | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680911 | ATTAAGTGAAGTAAC[-/AA]ATGTAAAAATACCTT | 4215 |
| rs765901563 | snp | C/T | 6.59131e-05 | 0.0057404 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685629 | AGGGTAATGCATAGG[C/T]ATTTTTGGAATTGAT | 4215 |
| rs765916440 | snp | A/C | 4.95806e-05 | 0.00497874 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634742 | AGCTCAGCCCTTCTG[A/C]ACAGCCCCACAGTAA | 4215 |
| rs765946080 | in-del | -/AGTTTTTTTTT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650695 | GAGAGAGAGAGAGAG[-/AGTTTTTTTTT]TTTTTAGACAGGGTC | 4215 |
| rs765946549 | snp | G/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683238 | GGCTATGAGAAGCCC[G/T]TTGTACTCTTCTTCC | 4215 |
| rs766032902 | snp | C/T | 2.38268e-05 | 0.0034515 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689750 | TGTGAGGAGCTGTCC[C/T]TGGCTAGGAGGAGAC | 4215 |
| rs766044562 | snp | C/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690714 | CCTAGACAAGTATCT[C/G]TCCCCAGCTCTCAGC | 4215 |
| rs766097976 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632040 | TTCATTCAGTACCAT[A/G]TTACATTGTACTGTG | 4215 |
| rs766156318 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695442 | CGCATGCGCCAGTTG[G/T]GCCTGGACCCTCCTG | 4215 |
| rs766174733 | snp | A/G | 4.94637e-05 | 0.00497287 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691187 | ATGGCTGTCTGCGGG[A/G]CCGCGCTGAGAAGAC | 4215 |
| rs766216811 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658987 | GTGATCCACCCGCCT[C/T]GGACTCCCAAAGTGT | 4215 |
| rs766297432 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647439 | GTTGGAGCCCAATTA[C/T]GCAGTTAGGCTCTCC | 4215 |
| rs766298485 | snp | C/T | 3.30732e-05 | 0.00406638 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693546 | GGGGTTCTCTCTTTC[C/T]AGGAGCCTGGGCTGC | 4215 |
| rs766309886 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663651 | TCCTTGAATATTGAG[C/G]ATTATCTTAGAACAA | 4215 |
| rs766313267 | snp | A/G | 3.31214e-05 | 0.00406935 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692204 | GGAGAAAATGCAAGA[A/G]GGTCCAGGGTTGCAG | 4215 |
| rs766360545 | in-del | -/AG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650659 | CTCTCTGTCTCTTAT[-/AG]AGAGAGAGAGAGAGA | 4215 |
| rs766381940 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634181 | CTATAACTCATTTGT[A/G]TTCAAAGCCACTTTT | 4215 |
| rs766417391 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686167 | GCCACTCCCTCGCCT[C/T]TGCCTCATTATGCCC | 4215 |
| rs766438532 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685246 | AATGAGCCAAGAACA[C/T]GCCAACAAGAAAAGC | 4215 |
| rs766467416 | in-del | -/GGGA | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678788 | TAATCCCAGCACTTT[-/GGGA]GGCTGAGACAGGCAG | 4215 |
| rs766476291 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646117 | TGTTCATGTATGCCA[A/C]AGTTCTCAGATAGCA | 4215 |
| rs766478396 | snp | A/C | 2.46917e-05 | 0.00351358 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689512 | TAGCCTGGGGTGTGA[A/C]TTGCTCTCCTCTGGC | 4215 |
| rs766496256 | snp | C/T | 1.73294e-05 | 0.00294353 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689666 | CAATACCTGGACCCC[C/T]GTGGGCGCCTGCGGA | 4215 |
| rs766591987 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637046 | GGGACAAACTTTCTG[A/G]AAGAGGAGATTACCA | 4215 |
| rs766612733 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670855 | AGGGGAGGGCAGGAT[A/G]AAGCTGGGGAGGGAG | 4215 |
| rs766614565 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664817 | GGCATAGTCCCACCT[G/T]CCTCCTTCCTCTTTT | 4215 |
| rs766621380 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670831 | GCTGGAGAGCTGGGA[A/G]CAAGGGGAAGGGGAG | 4215 |
| rs766650976 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629778 | ATGACAGTGCCAAAC[-/T]TTTCCACTAGTGTGT | 4215 |
| rs766667005 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627349 | CCTGGTAGCTTCTAA[A/G]TGTGTCAGACCACTC | 4215 |
| rs766678195 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674488 | CTCCCAAATAGCTGG[A/G]ACCACAGGTGCTTGC | 4215 |
| rs766728609 | in-del | -/G | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63670770 | GAGCAGAGACTTGAT[-/G]GCAAGAGGAAGTGTG | 4215 |
| rs766758255 | snp | C/T | 4.94442e-05 | 0.00497188 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632724 | GAACGATCTGGTGGC[C/T]CTCCAGATGAACCGA | 4215 |
| rs766786491 | snp | C/G | 1.65132e-05 | 0.00287339 | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690995 | TCTCCAACTGCAGTT[C/G]CCAAGGCAGATCCCT | 4215 |
| rs766851783 | in-del | -/T | 0.000436685 | 0.01477 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634691 | AATTATTAACCTCAG[-/T]TTTTTTTGTTTTTAA | 4215 |
| rs766858407 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641593 | CACCAACCTAAGTTC[A/G]AGGTTACACAGCTAG | 4215 |
| rs766884490 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640379 | GAGTTTGAGATTACA[A/G]TGGGAAAAAACCTCA | 4215 |
| rs766899064 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692164 | CTCTCCAGCAGCTCT[C/T]AGTGACCCGGGGGTG | 4215 |
| rs766920130 | snp | A/G | 1.65463e-05 | 0.00287626 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652574 | TTATAGCGTTCAGCC[A/G]GCCTGTGAAATATGA | 4215 |
| rs766946632 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640604 | ATGGTCTTTCTTTAT[G/T]CTACTTATTGTGAAT | 4215 |
| rs767043506 | snp | G/T | 0.00185857 | 0.0304275 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645985 | TGGCAATGGCAGGAG[G/T]GACACATTCCAGAGA | 4215 |
| rs767078475 | snp | C/T | 3.32508e-05 | 0.00407729 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689780 | CTGCCCAGGTGGTCT[C/T]AGACAAGCTACGGGG | 4215 |
| rs767105021 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693303 | TAGCTAATACAGTTA[C/T]TGTAGAGTTCTTTCT | 4215 |
| rs767116028 | snp | C/T | 3.29859e-05 | 0.00406102 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634769 | GTAACAACAAGCTCA[C/T]GTGCAGGGGCCAGTG | 4215 |
| rs767141076 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655257 | GAACTCACTCACTAT[C/G]AGGAGAACAGCAGCA | 4215 |
| rs767262754 | snp | A/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694680 | CAGAAGGGGAGATGG[A/G]CGACACGGTCGGGGC | 4215 |
| rs767317282 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688586 | CTGACAACAGACAGG[A/G]ATACTCAGGTGAGTT | 4215 |
| rs767364978 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681527 | TATTCTGGTTTCTGT[C/T]TTGTGTCAAGGTTTT | 4215 |
| rs767376926 | snp | C/T | 1.69198e-05 | 0.00290854 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667088 | ACCCTTTTTTCTCCC[C/T]CTCTATTTTATCTGC | 4215 |
| rs767384308 | in-del | -/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621995 | GCCTCACGCCGGAGC[-/T]GTGATTGGAACAACC | 4215 |
| rs767395872 | snp | C/G | 1.6486e-05 | 0.00287102 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690316 | CCTGGGCCAGGGTGC[C/G]TTCGGCAGGGTCTAT | 4215 |
| rs767418519 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632271 | CCGAGGCAGGAGGAT[C/T]ACTGGAGTCCAGGAG | 4215 |
| rs767423336 | snp | C/G | 0.000190567 | 0.00975946 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63622793 | CGCCCCGGCCTGTGC[C/G]CGCGCTGCTTCGCGA | 4215 |
| rs767428124 | in-del | -/AT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632862 | GTTTTCAAATGGGAA[-/AT]ATATACGAAAAGCCA | 4215 |
| rs767436855 | snp | A/G | 3.44448e-05 | 0.00414984 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689630 | CTGAGCACAAATGGC[A/G]AGAACATGGGTCTGG | 4215 |
| rs767526575 | snp | A/T | 8.01266e-05 | 0.00632905 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657765 | CTTCTGTTTTATATT[A/T]TTTTCCTTTTCTATG | 4215 |
| rs767527350 | snp | C/T | 1.66125e-05 | 0.00288201 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652636 | GGACAACCTCTTGAT[C/T]TACATTACATGAACA | 4215 |
| rs767535439 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651459 | AGCCTAGGTGACAGA[A/G]CGAGACTCTGTTTTG | 4215 |
| rs767538814 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673865 | CATTGAGCCAAGATC[A/G]TGTCACTGCACTCTA | 4215 |
| rs767587606 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672582 | TATTGGAAATTGTTA[C/T]GTTGAAACCATGCAC | 4215 |
| rs767594482 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621614 | CCAGAGGGTGTGGCC[C/T]TGGAGGTGTGAGACA | 4215 |
| rs767597815 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634916 | GATTTGTAAAAAGCA[C/T]TGGTTACCCGTGACC | 4215 |
| rs767608393 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635630 | AGATGTTGGGGAGAG[A/G]TATTTATAGCCTAGT | 4215 |
| rs767678308 | in-del | -/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676821 | CTGGAGACCAGGTGT[-/G]GGGCCTCTGCTAACA | 4215 |
| rs767718792 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63649566 | CTGGGACAACAGGCA[C/T]ACTGCCATAGCCAGG | 4215 |
| rs767733452 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686337 | TTGTCTTGCCTAATA[A/G]ACCTGAGCACTGATG | 4215 |
| rs767755283 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652497 | TACTCAGACCATTGC[G/T]TTTTAAACCCTACGT | 4215 |
| rs767800646 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651589 | ACCCAGCTTCAACAT[G/T]ACTAACATTTTCCCA | 4215 |
| rs767808270 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667089 | CCCTTTTTTCTCCCC[C/T]TCTATTTTATCTGCC | 4215 |
| rs767838559 | in-del | -/AGAGGG | 1.65625e-05 | 0.00287766 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692201 | ATGGGAGAAAATGCA[-/AGAGGG]TCCAGGGTTGCAGCC | 4215 |
| rs767938803 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665021 | AAAATCTCCACAGGC[A/T]GCTGGGCATGGTCGC | 4215 |
| rs768027016 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665768 | TGGTTCTGACTTCCC[A/G]TTAGAGCAAGACAGT | 4215 |
| rs768081637 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628836 | AAATTAAGTATTAGG[A/G]TAGATTAAATGGCCT | 4215 |
| rs768137544 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677852 | CAAAGAAAGAAAGAT[A/G]CATGGCACTGTGCTT | 4215 |
| rs768143769 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658506 | GATTCCTGGAGGCCC[A/G]CATTTCACAAGAATG | 4215 |
| rs768202063 | snp | A/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694969 | AAGCAGCTTAGAGTT[A/G]GCCATATTTACCTCA | 4215 |
| rs768206609 | snp | C/T | 1.6945e-05 | 0.00291071 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691086 | GAGCTGAGGCGACCA[C/T]TGACCCCTCCCCTAG | 4215 |
| rs768210716 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674513 | GCTTGCCACCATACC[C/T]GGCTAATTTGTTTTT | 4215 |
| rs768255119 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638349 | AGTACAGAATCAGAG[C/T]GAGGATAAGAAGAAT | 4215 |
| rs768352845 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636839 | AGGCCAAGAAGACTG[C/T]GTTGGTGGTCAAGTC | 4215 |
| rs768395090 | snp | C/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63695012 | GTCCTTTCTTCCGGC[C/T]CCTCCCCTCCAAAAT | 4215 |
| rs768403331 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623285 | CGCGCCCCAGCGCAG[C/G]GGGGAGGGCGTGCGG | 4215 |
| rs768407017 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673188 | TTTGGATTGAAAATC[A/G]GCTTTCTCTCACTTT | 4215 |
| rs768423193 | snp | C/T | 9.89772e-05 | 0.00703412 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691161 | GCAGCATGAGCGCAT[C/T]GTGCAGTACTATGGC | 4215 |
| rs768429274 | snp | C/T | 1.76649e-05 | 0.00297189 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681878 | TGAGGGGGAGTTCAT[C/T]CCAGAGACCAGCGAG | 4215 |
| rs768526656 | in-del | -/TATTTT | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676245 | TCAGAAAACCTTTGC[-/TATTTT]TCCCCCCAGACCCTC | 4215 |
| rs768560610 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651336 | AAAAATAAAAAATTA[C/G]TCGGTGCATGCCAGT | 4215 |
| rs768611946 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665496 | TTGAGGGTTTAGATA[A/G]TATGTCCTTTGGTAC | 4215 |
| rs768762681 | snp | A/C | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676285 | GTCTGTAGTGCTGGC[A/C]TCCTGTGAGCTAGTC | 4215 |
| rs768764439 | in-del | -/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663271 | ACTTTGGGAGGCTGA[-/G]GTAGGTGGATCCCTT | 4215 |
| rs768781864 | snp | A/C | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666982 | TCCAGACAGGTGCGG[A/C]TCAAGGCTTCCCAGT | 4215 |
| rs768845358 | snp | A/C/G | 1.64855e-05 | 0.00287097 | synonymous-codon, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667039 | CAGCCCCCCGAGCCC[A/C/G]GAAGCAGGCACCTCT | 4215 |
| rs768847997 | snp | A/G | 1.65203e-05 | 0.002874 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690288 | CCCCCATCAACTGGC[A/G]CCGGGGAAAGCTCCT | 4215 |
| rs768864371 | snp | A/G | 1.65261e-05 | 0.0028745 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690395 | CAATTTGATCCAGAC[A/G]GTCCTGAGACAAGCA | 4215 |
| rs768979048 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654802 | CAGCACTTTGGGAGG[C/T]TGAGGCGGGCAGATC | 4215 |
| rs769017181 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647012 | TGAGGTCTTCCTACT[G/T]TAAGAGTCTCACCAC | 4215 |
| rs769028000 | in-del | -/TTC | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635528 | TGACCAAGAGGGATA[-/TTC]TTCAGCAAAATTCTG | 4215 |
| rs769037639 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680546 | GATCATGGAAAGCAA[C/T]ACAGCCAGTCAGAAA | 4215 |
| rs769042361 | snp | C/G | 3.30737e-05 | 0.00406642 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693679 | TCCCACATCTCTGAA[C/G]ATGGCCGGGACTTCC | 4215 |
| rs769056629 | in-del | -/AAAACAA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626077 | AGAGACCCTGTCTCT[-/AAAACAA]AAAACAAACAAAAAA | 4215 |
| rs769069033 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655911 | CTCCCATTCCATAAG[C/T]AGTTTTGAGATTTTA | 4215 |
| rs769069632 | in-del | -/TCTGGAAAATGCAT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669171 | TTCTAACTGGAATGA[-/TCTGGAAAATGCAT]TCTGGAAAATGCATT | 4215 |
| rs769092579 | snp | C/G | 3.3284e-05 | 0.00407932 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691898 | TGGAGTCCCCAGGAC[C/G]TGGGTTCAAGTCTAC | 4215 |
| rs769094464 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668144 | TGCCCTTATCCATAT[A/G]GGTAGAATTGCTTCA | 4215 |
| rs769124862 | in-del | -/GTTGCCCAGGC | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628397 | CGGAGTTTCGCTCTT[-/GTTGCCCAGGC]TGGAGTGCAATGGCA | 4215 |
| rs769146431 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665229 | GGAGTACAGTGGTGC[C/G]ATCTCGGCTCACTGC | 4215 |
| rs769154360 | snp | C/T | 4.95642e-05 | 0.00497792 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657837 | ATCTTGATAAAGCAA[C/T]TGACATTTTAGATAG | 4215 |
| rs769155656 | snp | A/G | 9.68007e-05 | 0.00695636 | utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622728 | GGAGGTGACACTCAC[A/G]GACCTTAGCCACCGC | 4215 |
| rs769219525 | in-del | -/T | 1.82583e-05 | 0.0030214 | frameshift-variant, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689705 | AGCGAGAATGCCCTC[-/T]CTGTGCAGGAGAGGA | 4215 |
| rs769296805 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696537 | TGGGGTGGTCCCAAC[A/G]GGGCTGATTTACCAG | 4215 |
| rs769330972 | snp | C/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682733 | GCAGCTTCTTCAAAG[C/G]CAGCAGGAGAATCTT | 4215 |
| rs769354195 | in-del | -/AAAT | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673918 | TCTCAAAAAAATAAA[-/AAAT]AAATAAAAATTATCC | 4215 |
| rs769384123 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624656 | CTCCTGTCAGTTTTA[C/T]GTGAAGACACATGTA | 4215 |
| rs769418881 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642004 | AGAAGAATGGCTGGC[C/T]GGAAGGCATTGAATC | 4215 |
| rs769419918 | snp | C/T | 4.73003e-05 | 0.00486291 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689749 | GTGTGAGGAGCTGTC[C/T]CTGGCTAGGAGGAGA | 4215 |
| rs769437850 | snp | A/C | 1.89023e-05 | 0.00307422 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652703 | GAGGGGCAGATGCCT[A/C]CCTTTTTTCTCTCTG | 4215 |
| rs769441109 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63695213 | CAAGCCAAAGCCTTC[A/G]TTGTATGTTGACGAT | 4215 |
| rs769487380 | in-del | -/CTTA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624054 | TGTTCATTTGCTGGG[-/CTTA]CTGTTTCCTTCTCAT | 4215 |
| rs769511679 | snp | A/C | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674789 | ATCGAGTCCAGGTAG[A/C]GGGTTTATAATACTT | 4215 |
| rs769570855 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673628 | AACTAAAGGACTTGT[C/T]GGCGGGGTGCAGTGG | 4215 |
| rs769581427 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639555 | GAAAAAGGTGATTGA[A/G]ATGGTTGGAACTGTA | 4215 |
| rs769587395 | snp | C/T | 1.65141e-05 | 0.00287346 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634842 | GCCAAAATGTACTTT[C/T]AAATCTGCTACTCAT | 4215 |
| rs769629755 | snp | A/G | 0.000230798 | 0.0107399 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688547 | CCTTCCGGAAATCAC[A/G]AATGTCCCGTGCCCA | 4215 |
| rs769639874 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661777 | ATAAAACAAACCTGA[C/T]TGGGCAGAATAGCTT | 4215 |
| rs769700486 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677632 | CCTACAAACCCTCTG[C/T]TGGCCAAGCGGCATT | 4215 |
| rs769730802 | snp | C/T | 1.65441e-05 | 0.00287607 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693538 | GGTGACACGGGGTTC[C/T]CTCTTTCCAGGAGCC | 4215 |
| rs769737288 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653182 | TCACTCCACCCCAAC[A/G]GTCCTTATTTACTTC | 4215 |
| rs769763927 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688108 | TTGCTACCTCACAGC[A/G]TTCTGAGGATTAAAT | 4215 |
| rs769773516 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663955 | CAGATTTTAAAAAGG[G/T]CTTTAGGCCGGGCGC | 4215 |
| rs769822935 | snp | A/C | 1.66178e-05 | 0.00288247 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691283 | AAAAGAGGGCCTGAC[A/C]TGGGGGCTGGGGCCT | 4215 |
| rs769872608 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656793 | CGTATGAGTGTATTA[A/G]TCTGTTCTCACGCTG | 4215 |
| rs769961099 | snp | C/T | 1.65737e-05 | 0.00287864 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690405 | CAGACAGTCCTGAGA[C/T]AAGCAAGGTACACTT | 4215 |
| rs769965231 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642711 | AGAATGAAAGCTGTT[A/G]TGTGTGTGTGTGTTT | 4215 |
| rs769988237 | snp | A/T | 1.67621e-05 | 0.00289495 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667078 | GAGTATTTCAACCCT[A/T]TTTTCTCCCCCTCTA | 4215 |
| rs769994067 | in-del | -/C | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696702 | CTCCAAGAGCCACCT[-/C]TCCAGTACCCCCTTG | 4215 |
| rs770006279 | snp | A/G | 1.6495e-05 | 0.0028718 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632694 | AGACGAACAGGAGGC[A/G]TTGAACTCAATCATG | 4215 |
| rs770006698 | snp | C/T | 1.79191e-05 | 0.00299319 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63681778 | TAGGCTCCCAGAACC[C/T]TGGCCGAAGCTCACC | 4215 |
| rs770132803 | snp | A/G | 5.09554e-05 | 0.00504729 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689504 | CCGCCTCGTAGCCTG[A/G]GGTGTGACTTGCTCT | 4215 |
| rs770197493 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627066 | GAGATACAAGTAATA[G/T]CTCAGTCTGGAAGAG | 4215 |
| rs770269753 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684258 | GACTCAGCAGTTTTC[C/T]CCAAGGCCTCTTGTG | 4215 |
| rs770329064 | snp | G/T | 1.66852e-05 | 0.0028883 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691909 | GGACCTGGGTTCAAG[G/T]CTACCATTGAGTGCC | 4215 |
| rs770345423 | in-del | -/AG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656748 | CTTATTTGTACCCTC[-/AG]GGACCTTCTATTTAA | 4215 |
| rs770352176 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688570 | CGTGCCCAGAGCTTC[C/T]CTGACAACAGACAGG | 4215 |
| rs770382809 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685681 | CTCTGGAGGCCCAGG[A/G]TTAAAACATCATGCT | 4215 |
| rs770435278 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668915 | ATTCCGCCTGGGAGA[C/G]AGGGGCTTTCACAGA | 4215 |
| rs770461952 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669744 | GGCGTGAGCCACCAC[A/G]CCTCAACCTATCATG | 4215 |
| rs770553404 | snp | C/T | 1.67494e-05 | 0.00289386 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691685 | ATGGGCTTGCCCCTC[C/T]ACCAGCCCTCCCCTG | 4215 |
| rs770566362 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676064 | CTGGTTTTTCCATTC[A/G]GTTCCTCTGATAGCC | 4215 |
| rs770567706 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634673 | ATGTTGCACGAAGGA[C/T]ACAAATTATTAACCT | 4215 |
| rs770594407 | snp | C/T | 1.64955e-05 | 0.00287184 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691765 | GTTGAAGGCTTACGG[C/T]GCTCTGACAGAGAGC | 4215 |
| rs770640103 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626590 | GCATTTGACTTTGAG[A/G]TTTAGCAAAGGTTCA | 4215 |
| rs770682931 | snp | A/C | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696613 | GTTCCCGGAGCTTTC[A/C]TGATATTTGGTAGGG | 4215 |
| rs770706062 | snp | A/G | 4.96504e-05 | 0.00498224 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693701 | GGGACTTCCTGAGGC[A/G]CATTTTTGTGGAGGC | 4215 |
| rs770755395 | snp | A/G | 1.66515e-05 | 0.00288539 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63646066 | GTTCGAGCACAACGG[A/G]GAGAGGCGGTAAGTC | 4215 |
| rs770763918 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650934 | GCTCCTAGCCTCAAG[C/T]GAGCCTCCTACCTTG | 4215 |
| rs770852623 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665586 | TTCAGGCAGGTGGCA[A/G]GGTGCTCATCATGCA | 4215 |
| rs770865966 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651080 | CTGATTATTTTTAGT[C/T]ATTTCTGTTCTAGAG | 4215 |
| rs770892039 | snp | G/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674891 | GAATGTTGAAAGGAT[G/T]AGGGTAGATTATAGC | 4215 |
| rs770948105 | snp | C/T | | | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696004 | CAGTTCCTGGCAGCC[C/T]CAGGCTTGCTGTGGG | 4215 |
| rs771018451 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644458 | TGACCTCCAGTGATC[A/T]GCCCGCCTCGGCCTC | 4215 |
| rs771041240 | snp | C/G/T | 4.95179e-05 | 0.00497563 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685467 | AAGCCTGGGTCACTG[C/G/T]GGGGAATTGGGGCTG | 4215 |
| rs771067940 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666473 | ACTCTGTATCAATCA[A/G]TCAGTCAATAAGATA | 4215 |
| rs771072364 | snp | A/C | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680066 | ATGAGTCAGGTACTT[A/C]CCTAGGTCTCCAGCT | 4215 |
| rs771075974 | snp | G/T | 3.32094e-05 | 0.00407475 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692334 | TGTATGTCGGGGACG[G/T]GCATGCGCTCCGTCA | 4215 |
| rs771129953 | snp | A/G | 1.65138e-05 | 0.00287343 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632843 | GTGAGATTTGTTGGG[A/G]AGGGGTTTTCAAATG | 4215 |
| rs771133315 | in-del | -/TTAC | | | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696277 | GGCCAGTGTTGCGCA[-/TTAC]TTACTTACAATAAAA | 4215 |
| rs771141241 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628680 | TATCTTTTTTTTCAT[A/G]CAACTTTGTATTTGT | 4215 |
| rs771142287 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627765 | TTTTTTGTATTTTTT[A/G]TAGAGATGGGGTTTT | 4215 |
| rs771152078 | snp | C/T | 3.35464e-05 | 0.00409537 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634698 | TAACCTCAGTTTTTT[C/T]GTTTTTAAAGAAAAA | 4215 |
| rs771267664 | snp | C/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693939 | ACTGGGGCTCAGAGC[C/T]GGGGTGGGGTGGCTG | 4215 |
| rs771271392 | snp | A/G | 1.76387e-05 | 0.00296969 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689687 | CGCCTGCGGAGTGCG[A/G]ACAGCGAGAATGCCC | 4215 |
| rs771273140 | snp | A/C | 2.06524e-05 | 0.00321337 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657745 | AAGTGAAACATTGAG[A/C]TAAACTTCTGTTTTA | 4215 |
| rs771375006 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693228 | AGAACTGTAAGATGA[C/T]ACATTTGTGTTGTTT | 4215 |
| rs771402300 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656179 | AGGTTGCTGTGAGCC[A/G]AGATTGTGCCACTGC | 4215 |
| rs771406233 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671341 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 4215 |
| rs771408071 | in-del | -/CTGGTGCTTTGCAGTGTATTTATGCTGAGTAAAGAATGTGTAC | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653297 | TACAATCAGCTTAGG[lengthTooLong]CTCGAGGAAATTGAG | 4215 |
| rs771464819 | snp | C/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693904 | CAGCCCAGCCAGCGT[C/T]GGTCTGTGCCCCTTC | 4215 |
| rs771465083 | snp | A/C | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677772 | TTTGGGAGGCTGAAG[A/C]AGGAGGATCCCTTGA | 4215 |
| rs771477615 | snp | C/T | 0.000812135 | 0.0201347 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689603 | TTCACCCTGGTGCCC[C/T]CCAGCCGCTCCCTGA | 4215 |
| rs771479954 | in-del | -/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639562 | GTGATTGAGATGGTT[-/G]GAACTGTAGAGGAAC | 4215 |
| rs771488402 | snp | A/G | 1.67248e-05 | 0.00289173 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646078 | CGGGGAGAGGCGGTA[A/G]GTCTGCCTTCTGATG | 4215 |
| rs771511156 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673092 | AGGCTACTCAGTTCA[C/T]ACTGGAACATTTGCA | 4215 |
| rs771584521 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659638 | CCCGGGTTCAAGCAA[-/T]TCTTCTGCCTCAGCC | 4215 |
| rs771594507 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634876 | GCAACAGCAGAATTC[A/G]CTTCCCAGACAAGTT | 4215 |
| rs771618022 | snp | A/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621039 | AGAAAAGAAATAGGG[A/G]AGAGCCCAAGGTAAT | 4215 |
| rs771634211 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657211 | AATTTGGAAAAGAAT[A/G]TGGGGGCTGTAACTG | 4215 |
| rs771675922 | snp | A/T | 1.65364e-05 | 0.0028754 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632661 | AAGTGTCTTAGTCCA[A/T]GTGCTCTCTTTCATT | 4215 |
| rs771693753 | snp | A/G | 0.000131809 | 0.00811708 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688807 | GGGAAACTCAGCTTT[A/G]TGACAAAGGGGTCAA | 4215 |
| rs771710129 | snp | C/T | 1.65957e-05 | 0.00288055 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688904 | CTTCTTCACCTGCTC[C/T]CTGCTGGCTGCCTCA | 4215 |
| rs771714111 | snp | A/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621149 | TTATTCTGGAGCCTG[A/G]CATATTACACTGGAA | 4215 |
| rs771727927 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652199 | TCCCCAAGTCCCAAC[A/G]GCCCCAGTGTGTATT | 4215 |
| rs771792889 | snp | A/T | 2.36588e-05 | 0.00343931 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691035 | CTAACTAGGGCAAGC[A/T]GAGCTGAACCCAGGC | 4215 |
| rs771819825 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636757 | CTGTTTGTCAGCGAC[A/G]ATGAGGAGGAAGACA | 4215 |
| rs771943327 | in-del | -/A | 9.04429e-05 | 0.00672408 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681908 | GCAGTGCGTGAGTAT[-/A]GGGGGGCTGGGATAT | 4215 |
| rs771945109 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678132 | CGCTTCGGCCCCACC[A/G]TAAAGTCACTTTATG | 4215 |
| rs771984420 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662119 | TCTCAATAATAATAA[C/T]ATTGGGCTGGGCATG | 4215 |
| rs771996520 | in-del | -/CACT | 0.000389997 | 0.0139587 | utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622721 | CGGCTGCGGAGGTGA[-/CACT]CACGGACCTTAGCCA | 4215 |
| rs771998322 | snp | C/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680645 | TTGCTCAGTGACTTA[C/G]AAAGTGTGTCATTTG | 4215 |
| rs772050753 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637946 | GGGCCTTGGCTATCA[-/T]TTCTAGAGGAAGAGA | 4215 |
| rs772088393 | snp | A/G | 1.79968e-05 | 0.00299968 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652520 | CCCTACGTTTTAAGT[A/G]TACAATTAACCAACC | 4215 |
| rs772089107 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693450 | GCCTGTCCTGCACCT[C/G]AGCTTGCTGTGAGAA | 4215 |
| rs772104628 | in-del | -/ACAGCATGTC | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645770 | TGTATGAAGCTAGAA[-/ACAGCATGTC]ACAGCATGTCACAGC | 4215 |
| rs772138667 | snp | A/G | 1.66299e-05 | 0.00288352 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634718 | TTAAAGAAAAAACAC[A/G]ACAGCAGCAGCTCAG | 4215 |
| rs772142006 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653229 | CAGGAAGGAATTCTT[C/T]TGAATGTCAGTTTCT | 4215 |
| rs772155457 | snp | A/G | 4.95168e-05 | 0.00497553 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634833 | CCTGTTAAAGCCAAA[A/G]TGTACTTTTAAATCT | 4215 |
| rs772180640 | snp | C/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690078 | CTCTGCTTCTTAGGA[C/G]TCTGACTTCAGGTCC | 4215 |
| rs772210962 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667835 | TTGAATCCACAGATG[C/T]AGAACCTGGAGATAT | 4215 |
| rs772217096 | snp | A/G | 4.96644e-05 | 0.00498294 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693531 | GCTGAGGGGTGACAC[A/G]GGGTTCTCTCTTTCC | 4215 |
| rs772222539 | snp | A/G | 5.78007e-05 | 0.00537559 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689721 | CTGTGCAGGAGAGGA[A/G]TGTGCCAACCAAGTG | 4215 |
| rs772242272 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631556 | ACGATCAACAGATTT[A/T]TTCATTTTCAATCTC | 4215 |
| rs772270520 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656401 | TGAGGTCAGGAGTTC[A/G]AGACCAACCTGACCA | 4215 |
| rs772305243 | snp | A/G | 3.30513e-05 | 0.00406504 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693650 | CCACCCAGCCCACCA[A/G]TCCTCAGCTGCCCTC | 4215 |
| rs772322521 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666972 | CTCTGGGGTGTCCAG[A/G]CAGGTGCGGATCAAG | 4215 |
| rs772426990 | snp | C/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694715 | GGCCTGGCCAGTGCC[C/T]TGATCCCAGAGAGCC | 4215 |
| rs772436082 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658397 | GTTGGGGGCCTCTTA[C/T]AACTTATCAGCTGTT | 4215 |
| rs772456755 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | MAP3K3 | GRCh38.p7 | 17:63694072 | GTGGGCCCCACCCTC[A/G]GGGATGTGTCCTGAC | 4215 |
| rs772489241 | snp | A/G | 1.66252e-05 | 0.00288311 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692341 | CGGGGACGGGCATGC[A/G]CTCCGTCACTGGCAC | 4215 |
| rs772489257 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653264 | TGCTTTCCCAGCTCC[A/C]AGAAGAATATTACAG | 4215 |
| rs772501406 | snp | C/T | 1.67351e-05 | 0.00289263 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690258 | TTTCCTTCTGCTCTC[C/T]TGTAGCTCCCAGTGC | 4215 |
| rs772507785 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679395 | ACCCTGGACTGGGCT[C/T]TTGAGCACCCTCTGC | 4215 |
| rs772520413 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680265 | TGGGAATTGCTGGGT[C/T]GTGGGAGAGAGGTAA | 4215 |
| rs772522423 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631886 | TCAAATGCTAGGCTT[C/G]TAAAACAACTTCTGT | 4215 |
| rs772544350 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631907 | CAACTTCTGTTCAAA[G/T]CAGTTACCTGAGGCC | 4215 |
| rs772547540 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63643184 | GTAACAAAAAGAAAT[A/G]TACCATACTAATGTA | 4215 |
| rs772555456 | snp | A/C | | | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695676 | TCCCCAGTCCCTGTT[A/C]CCCAAGAGGATACAG | 4215 |
| rs772582224 | in-del | -/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627782 | AGAGATGGGGTTTTG[-/C]CATGTTGCCCAAGCT | 4215 |
| rs772585551 | snp | A/C | 1.67024e-05 | 0.0028898 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691701 | ACCAGCCCTCCCCTG[A/C]GGGGACTCCTCTGAC | 4215 |
| rs772622236 | in-del | -/GCC | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693161 | ACAGGAACCAGCCCT[-/GCC]GCCACCTTGACTTTA | 4215 |
| rs772638296 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665377 | CCACTGTGCTAGCCA[C/G]GATGGTCTTGATCTC | 4215 |
| rs772686374 | snp | C/T | 1.65589e-05 | 0.00287736 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657881 | AAAAGCCTTAGGATA[C/T]TGCTGTTGTCCCAGG | 4215 |
| rs772715893 | snp | C/T | 3.80373e-05 | 0.00436087 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652704 | AGGGGCAGATGCCTA[C/T]CTTTTTTCTCTCTGT | 4215 |
| rs772772513 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668417 | TGGTTGAGGATGGAG[A/G]GCTAGTACCCTAGCA | 4215 |
| rs772796223 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648849 | TTACAGTCTCAATGG[A/G]TTTCCTAGTGGAGAT | 4215 |
| rs772818922 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633164 | ACCTGGAAGGCAAAG[C/G]CTGCAGTGAGCCGAG | 4215 |
| rs772878870 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680995 | TTGTAGAGATGTTGA[A/G]AATCAAATGAGGTTA | 4215 |
| rs772922915 | snp | A/G | 1.6517e-05 | 0.00287372 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634845 | AAAATGTACTTTTAA[A/G]TCTGCTACTCATGCT | 4215 |
| rs773001096 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647333 | GTTAAATTGTCACTT[C/T]ACTGTTGCTACTTTT | 4215 |
| rs773047718 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691575 | ACTTGGGGTACTCTC[-/TT]TTCCAAACTGCCTGA | 4215 |
| rs773083246 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688556 | AATCACGAATGTCCC[A/G]TGCCCAGAGCTTCCC | 4215 |
| rs773115237 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658941 | AGGTTTCACCATGTT[C/T]GTCAGGCTGGTCTCA | 4215 |
| rs773173555 | snp | A/T | 1.64738e-05 | 0.00286995 | intron-variant, splice-donor-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685592 | AGGTCAGCAGACAGG[A/T]ATGGGACTGTGGGTG | 4215 |
| rs773224935 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689825 | CCCTGGGACCCTTAG[A/G]CTCAGCAGGTGGTGG | 4215 |
| rs773236784 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676578 | GAGTGTGTTGGTCAG[A/G]GTTCAGTTGTGCAGA | 4215 |
| rs773307665 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663867 | ACTGCACTCATTGAG[C/G]AAGACCCTGTCTCAA | 4215 |
| rs773334070 | snp | A/G | 6.59294e-05 | 0.00574111 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691813 | GCGGCAGATCCTGGA[A/G]GGCATGTCCTACCTG | 4215 |
| rs773357327 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632708 | CATTGAACTCAATCA[C/T]GAACGATCTGGTGGC | 4215 |
| rs773388654 | snp | A/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620588 | ATAGAGATTATTATA[A/G]TTAAGGAACTCCAGT | 4215 |
| rs773404820 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656086 | AGTACAAAAATTAGT[A/C]GGGTGTGGTGCCTCA | 4215 |
| rs773427937 | in-del | -/AA | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678253 | CAATATTTTTTTAAG[-/AA]AAAAAAATTGCCTTG | 4215 |
| rs773456886 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624718 | GGTGGCTGCAGTATA[G/T]TAGGCAAGCTAGTTT | 4215 |
| rs773503245 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677645 | TGTTGGCCAAGCGGC[A/G]TTTTGTATTCCTGGC | 4215 |
| rs773527166 | snp | C/T | | | utr-variant-3-prime, intron-variant | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695748 | GGTCTTACAGAGCTC[C/T]ACCCCCTGGGGTCTT | 4215 |
| rs773528129 | snp | C/T | 1.75428e-05 | 0.0029616 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689595 | GCAACTTGTTCACCC[C/T]GGTGCCCTCCAGCCG | 4215 |
| rs773535213 | snp | A/G | 3.29484e-05 | 0.00405871 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667009 | CAGTCCGCAGGGGAT[A/G]TAAATACTATCTACC | 4215 |
| rs773563402 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627123 | GAGTATGTTGCCTGG[C/T]AGCCTCCATACCACA | 4215 |
| rs773625164 | snp | C/T | 3.36729e-05 | 0.00410308 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667083 | TTTCAACCCTTTTTT[C/T]TCCCCCTCTATTTTA | 4215 |
| rs773698521 | snp | A/C | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692030 | TATGAGAGAATATTG[A/C]CAAGTTCCCTCTACA | 4215 |
| rs773704370 | snp | A/G | 5.01215e-05 | 0.00500582 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691912 | CCTGGGTTCAAGTCT[A/G]CCATTGAGTGCCTGC | 4215 |
| rs773704942 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669820 | CAAAAGATAATTACT[A/G]GCTGGGCATGGTGGC | 4215 |
| rs773722519 | snp | C/T | 3.32033e-05 | 0.00407438 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692332 | TCTGTATGTCGGGGA[C/T]GGGCATGCGCTCCGT | 4215 |
| rs773724439 | snp | G/T | 2.53264e-05 | 0.00355845 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689505 | CGCCTCGTAGCCTGG[G/T]GTGTGACTTGCTCTC | 4215 |
| rs773726395 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669660 | GGATTTCGCCATGTT[A/G]GCCAGGCTGGTATGA | 4215 |
| rs773787302 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655032 | CTCTGTCTCAAAAAA[C/T]GATTAAAAAAAATTA | 4215 |
| rs773871394 | snp | C/T | 1.64825e-05 | 0.00287071 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688575 | CCAGAGCTTCCCTGA[C/T]AACAGACAGGAATAC | 4215 |
| rs773889241 | snp | A/G | 1.64947e-05 | 0.00287177 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685637 | GCATAGGCATTTTTG[A/G]AATTGATGGGTTGAG | 4215 |
| rs773906536 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656184 | GCTGTGAGCCGAGAT[G/T]GTGCCACTGCACTCC | 4215 |
| rs773951930 | snp | A/C | 1.65479e-05 | 0.0028764 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634734 | ACAGCAGCAGCTCAG[A/C]CCTTCTGAACAGCCC | 4215 |
| rs773969492 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63671358 | CCTCCCGGGTTCAAA[C/T]GATTCTCTTGCCTCA | 4215 |
| rs773970807 | snp | C/T | 1.64936e-05 | 0.00287168 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690301 | GCGCCGGGGAAAGCT[C/T]CTGGGCCAGGGTGCC | 4215 |
| rs773975137 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63647630 | CTTATCAAGGTTTTG[A/G]AAATGGTGCATTCTC | 4215 |
| rs773990003 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683325 | ATTAGCTGCAGATTT[C/T]CTTTTTGGGCATTTT | 4215 |
| rs774139742 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633539 | ATAATGAGTGATTTT[A/G]TTATTACTGTTTACA | 4215 |
| rs774148273 | snp | A/G | 5.16889e-05 | 0.00508348 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693805 | ACACAGCTGCCGGTC[A/G]CCCTTTGCTGCATGG | 4215 |
| rs774157654 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662354 | CGGGAGGTTGAGGCC[A/G]CAGTGAGCCAAGATT | 4215 |
| rs774161042 | snp | A/G | 1.65466e-05 | 0.00287628 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693703 | GACTTCCTGAGGCGC[A/G]TTTTTGTGGAGGCTC | 4215 |
| rs774161839 | snp | A/C | 1.67156e-05 | 0.00289093 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691697 | CTCCACCAGCCCTCC[A/C]CTGAGGGGACTCCTC | 4215 |
| rs774171030 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660847 | GTGATCCGCCTGTCT[C/T]GGCCTCCCAAAGTGC | 4215 |
| rs774274934 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696742 | GCTACTGTTGCTTAA[C/T]CGAACCAAGATGATC | 4215 |
| rs774288034 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676129 | CCTGTGGGCCTGTGC[A/G]CAATAGCCGCTGGCA | 4215 |
| rs774406091 | snp | C/G/T | 1.64814e-05 | 0.00287061 | missense, synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632736 | GGCCCTCCAGATGAA[C/G/T]CGACGTCACCGGATG | 4215 |
| rs774512741 | in-del | -/A | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687933 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAGT | 4215 |
| rs774550730 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63626352 | AGTGCAAAAGTGTGT[-/A]AAGATATACAGGAGA | 4215 |
| rs774603132 | snp | A/G | 1.74567e-05 | 0.00295433 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63681817 | GCTATGTTCCTGAGC[A/G]GCAGCAGCACATTGC | 4215 |
| rs774617344 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629465 | TTGTTTTTAAAGAAT[A/G]CCACATTGGAGGAGT | 4215 |
| rs774639546 | snp | A/G | 3.31285e-05 | 0.00406978 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692206 | AGAAAATGCAAGAGG[A/G]TCCAGGGTTGCAGCC | 4215 |
| rs774649828 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662505 | GGTACCAGGGCAGGC[A/G]TCTATTATCTCCAGT | 4215 |
| rs774650001 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665592 | CAGGTGGCAGGGTGC[C/T]CATCATGCACCTCCT | 4215 |
| rs774794834 | in-del | -/C | 3.50607e-05 | 0.00418678 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691074 | CTAGGGCCCTGAGAG[-/C]TGAGGCGACCACTGA | 4215 |
| rs774801925 | in-del | GGGATGGAGTCTCA/TTTTTTTTGGGTTTTTCCTTTTT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662676 | TTTTTTTTTTTTTTT[lengthTooLong]CTCTGTCACCCAGGT | 4215 |
| rs774830564 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657245 | GCAACTTGATATTTT[G/T]AAGTAAATTAGTGTT | 4215 |
| rs774836957 | snp | C/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677837 | CACGCCACTGCACTC[C/G]AAAGAAAGAAAGATA | 4215 |
| rs774841853 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657148 | CCTTTTCTGCTTGTT[C/G]TATTAATGTCAGCAC | 4215 |
| rs774843454 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641661 | CTCCAGTGCTACATT[C/T]TTAACAACTACATAT | 4215 |
| rs774852925 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693325 | GTTCTTTCTGTCAAG[C/T]CTAAGTGATTCTCTT | 4215 |
| rs774926846 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679112 | GTCTTTCAAAAAGCA[A/G]CCCTCTGGCCAGGCA | 4215 |
| rs774934082 | snp | C/T | 3.55739e-05 | 0.00421731 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689692 | GCGGAGTGCGGACAG[C/T]GAGAATGCCCTCTCT | 4215 |
| rs774997840 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691780 | TGCTCTGACAGAGAG[C/T]GTGACCCGAAAGTAC | 4215 |
| rs775006018 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636777 | GGAGGAAGACAAGGA[A/G]GCAGCCCGGCTGTGG | 4215 |
| rs775019440 | snp | A/G | 3.31241e-05 | 0.00406952 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693722 | TTGTGGAGGCTCGCC[A/G]GAGACCTTCAGCTGA | 4215 |
| rs775100223 | snp | A/G | 1.73628e-05 | 0.00294637 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667106 | CTATTTTATCTGCCC[A/G]CATTTTAAAAAAGCA | 4215 |
| rs775102842 | snp | C/G | 1.68204e-05 | 0.00289999 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646090 | GTAAGTCTGCCTTCT[C/G]ATGAGTAGCTGTGTT | 4215 |
| rs775241912 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622721 | CGGCTGCGGAGGTGA[-/C]ACTCACGGACCTTAG | 4215 |
| rs775275166 | snp | A/C | 1.64868e-05 | 0.00287109 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688587 | TGACAACAGACAGGA[A/C]TACTCAGGTGAGTTC | 4215 |
| rs775281087 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620300 | TAATTTAAATTAAAA[C/T]TTTTTCCTGGCAGGG | 4215 |
| rs775293124 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688811 | AACTCAGCTTTATGA[C/T]AAAGGGGTCAAAGGT | 4215 |
| rs775316871 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651250 | GCACTTTGGAAGGCC[A/G]ACGTGGGAGGATTGC | 4215 |
| rs775404746 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634941 | GTGACCTGTGTTCAG[A/T]GCTTCTAGTCACCAT | 4215 |
| rs775405521 | snp | G/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63684973 | AATATTTTATTATAT[G/T]TAGATATCTATTACC | 4215 |
| rs775614606 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674906 | GAGGGTAGATTATAG[C/T]GACAACTGGGCAGTA | 4215 |
| rs775682833 | snp | A/G | | | intron-variant, downstream-variant-500B | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63681395 | ATTGAGCTGATGGGA[A/G]GAAATGGCATTAGTG | 4215 |
| rs775690887 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623628 | CACGTAGCATTTGAG[A/T]TGAATTATATTCCAT | 4215 |
| rs775721157 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688530 | TGTTTTCTCCAGCCC[A/G]TCCTTCCGGAAATCA | 4215 |
| rs775756240 | snp | C/G | 1.66081e-05 | 0.00288163 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634722 | AGAAAAAACACAACA[C/G]CAGCAGCTCAGCCCT | 4215 |
| rs775783118 | snp | C/G | 0.000137663 | 0.00829533 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689632 | GAGCACAAATGGCGA[C/G]AACATGGGTCTGGCT | 4215 |
| rs775784289 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629727 | AATTAGATTCTATAA[A/C]CCTGATTCACTTGTG | 4215 |
| rs775832508 | snp | C/T | 1.67198e-05 | 0.0028913 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657907 | CCAGGACAGAAACCA[C/T]GTAAGTAGCCCTTGT | 4215 |
| rs775841200 | snp | C/T | 6.65524e-05 | 0.00576817 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692345 | GACGGGCATGCGCTC[C/T]GTCACTGGCACACCC | 4215 |
| rs775855522 | snp | A/G/T | 3.30974e-05 | 0.0040679 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693534 | GAGGGGTGACACGGG[A/G/T]TTCTCTCTTTCCAGG | 4215 |
| rs775859438 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63653342 | AAAGAATGTGTACCT[C/G]GAGGAAATTGAGTTA | 4215 |
| rs775880039 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648621 | AAAAGGTCAGGAGTT[C/G]GAGACCAATATGGTG | 4215 |
| rs775881412 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63628610 | GGTGATCCACCTGCC[G/T]TAGCCTCCCAAAGTG | 4215 |
| rs775965990 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665889 | TTTTTCCTGGAGGAC[A/G]GGATATAGAGTTTGT | 4215 |
| rs775967141 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63645018 | GTTTGCCCTTTTGCA[A/G]TATCTCTTCCTCTTT | 4215 |
| rs775972736 | snp | G/T | 1.66974e-05 | 0.00288936 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691703 | CAGCCCTCCCCTGAG[G/T]GGACTCCTCTGACTT | 4215 |
| rs775982742 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644819 | TCCTCTTTCTTCCAA[A/G]CCACAGCCTATTAAT | 4215 |
| rs776079578 | in-del | -/A | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683544 | GAGGATTTGACTCCC[-/A]AGTGAGGACAGACTT | 4215 |
| rs776087539 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63679425 | CTGTAGATGCTTAGT[C/T]CCTGGTGCACTACCT | 4215 |
| rs776101395 | snp | C/T | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63695008 | GCTGGTCCTTTCTTC[C/T]GGCCCCTCCCCTCCA | 4215 |
| rs776120501 | snp | A/C | 2.57079e-05 | 0.00358515 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689498 | TACGTTCCGCCTCGT[A/C]GCCTGGGGTGTGACT | 4215 |
| rs776126405 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666976 | GGGGTGTCCAGACAG[A/G]TGCGGATCAAGGCTT | 4215 |
| rs776134734 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623305 | AGGGCGTGCGGGGCT[C/T]GGCTAGGAGGCGATT | 4215 |
| rs776163459 | in-del | -/CAC | 1.6486e-05 | 0.00287102 | cds-indel, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688860 | TACCACGTGTCTGTG[-/CAC]CACAAGGACTACAGT | 4215 |
| rs776200737 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652539 | AATTAACCAACCTTT[C/G]TTTCTGTTTCTTTTC | 4215 |
| rs776273449 | in-del | -/GAA | 0.000378922 | 0.0137593 | cds-indel, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63632769 | TGGATATGAGACCAT[-/GAA]GAACAAAGACACAGG | 4215 |
| rs776374696 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685529 | CAGATGCTGGATCCC[C/T]TGAGCAGTGCAGAAA | 4215 |
| rs776394763 | snp | G/T | 1.68778e-05 | 0.00290493 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646098 | GCCTTCTGATGAGTA[G/T]CTGTGTTCATGTATG | 4215 |
| rs776527114 | snp | C/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621364 | AATGTAAGCATACTA[C/T]AAAACAATACAAAGC | 4215 |
| rs776540419 | snp | A/G | 9.80344e-05 | 0.00700054 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691051 | GAGCTGAACCCAGGC[A/G]GGCAGAACTAGGGCC | 4215 |
| rs776550432 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652393 | AGGGTGAAAGGTAAC[A/G]GTAGAGAAGAGGAAA | 4215 |
| rs776556773 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635330 | TGGGAATCCTACCTA[A/G]GATTTCTGTTTTAGG | 4215 |
| rs776560365 | snp | A/G/T | 4.94926e-05 | 0.00497436 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691162 | CAGCATGAGCGCATC[A/G/T]TGCAGTACTATGGCT | 4215 |
| rs776631537 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673250 | AACAGATAAACACAG[A/G]TAAAATCTTTCATAT | 4215 |
| rs776633498 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63657520 | GACTATAAATGGGCA[C/T]AAGAGATCCTGTTGG | 4215 |
| rs776653116 | snp | C/T | 0.000115375 | 0.00759437 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690343 | CTATTTGTGCTATGA[C/T]GTGGACACGGGACGT | 4215 |
| rs776668831 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63676295 | CTGGCCTCCTGTGAG[C/T]TAGTCCCATCCCACC | 4215 |
| rs776723805 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625660 | ATCTGACCACCTATG[C/T]AGACTCTGAATAGTT | 4215 |
| rs776757066 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677589 | TTCCCTTGGTCCAGA[C/T]TTCCCCTAAACCTCC | 4215 |
| rs776758647 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662120 | CTCAATAATAATAAC[A/G]TTGGGCTGGGCATGG | 4215 |
| rs776806700 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63641107 | AACCACTTGTATATC[A/G]GGTACTGTTCTAATC | 4215 |
| rs776826899 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63668171 | TTCAAATTGAAGTGT[C/T]CTCTGAAGATCCTGA | 4215 |
| rs776910307 | snp | A/G | 1.65332e-05 | 0.00287512 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693682 | CACATCTCTGAACAT[A/G]GCCGGGACTTCCTGA | 4215 |
| rs776935191 | snp | G/T | 1.66521e-05 | 0.00288544 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691901 | AGTCCCCAGGACCTG[G/T]GTTCAAGTCTACCAT | 4215 |
| rs776940651 | snp | A/G | 1.64939e-05 | 0.0028717 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691840 | CCTGCACAGCAACAT[A/G]ATTGTTCACCGGGAC | 4215 |
| rs776978383 | snp | C/T | 5.32817e-05 | 0.0051612 | utr-variant-5-prime, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63622738 | CTCACGGACCTTAGC[C/T]ACCGCCGCCGCCATC | 4215 |
| rs776993223 | snp | C/G | 1.6476e-05 | 0.00287014 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689744 | ACCAAGTGTGAGGAG[C/G]TGTCCCTGGCTAGGA | 4215 |
| rs777002011 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688822 | ATGACAAAGGGGTCA[A/G]AGGTGGAACCTACCC | 4215 |
| rs777007673 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63678174 | TGGGTTTCCCTCTGC[A/G]CAATGTGGATGATGA | 4215 |
| rs777009629 | snp | C/T | 1.65165e-05 | 0.00287367 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690290 | CCCATCAACTGGCGC[C/T]GGGGAAAGCTCCTGG | 4215 |
| rs777128646 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63680554 | AAAGCAACACAGCCA[A/G]TCAGAAAAAGCTCTT | 4215 |
| rs777141398 | snp | C/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682479 | AGTCCAGGCATGACT[C/T]AAATGGGTCCTCTGC | 4215 |
| rs777211897 | in-del | -/AGAG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650659 | CTCTCTGTCTCTTAT[-/AGAG]AGAGAGAGAGAGAGA | 4215 |
| rs777255994 | in-del | -/TTTT | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621434 | CTCTGGGGTGGGATC[-/TTTT]TTTTCTTTTTCATAG | 4215 |
| rs777290169 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63663229 | AATGCTTGGCCAGGC[G/T]TGGTGGCTCATGCCT | 4215 |
| rs777463574 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650567 | CGCAGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 4215 |
| rs777487547 | snp | G/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677086 | CTACTGTGAGATGGG[G/T]TTATGCGGATATGTA | 4215 |
| rs777513148 | snp | A/C | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691335 | ATAGGAGTTTGAACA[A/C]CTGAGGCTCCAGAGG | 4215 |
| rs777542015 | snp | A/G | 1.66114e-05 | 0.00288192 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691285 | AAGAGGGCCTGACCT[A/G]GGGGCTGGGGCCTGC | 4215 |
| rs777548849 | snp | A/G | 1.65184e-05 | 0.00287384 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657840 | TTGATAAAGCAATTG[A/G]CATTTTAGATAGAAG | 4215 |
| rs777563450 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639578 | GAACTGTAGAGGAAC[A/G]CAGAGTGGGTTGGAA | 4215 |
| rs777575835 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661825 | AAATAAACACTGGGC[C/T]GGGCGCGGTGGCTCA | 4215 |
| rs777654870 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644397 | CTTTTTGTATTTTAA[G/T]TAGAGATGAGGTTTC | 4215 |
| rs777707925 | in-del | -/AG | 3.46063e-05 | 0.00415956 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646125 | TATGCCAAAGTTCTC[-/AG]ATAGCATTGAGTTCA | 4215 |
| rs777755586 | in-del | -/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669056 | TGGTGGGTTGAAGAA[-/C]CCCAGGGGCTTTGCA | 4215 |
| rs777761431 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654293 | ATTTACCTATTCTGA[A/G]CATTTCGTGTAGTGC | 4215 |
| rs777826815 | snp | G/T | 1.64977e-05 | 0.00287203 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691759 | AGACCAGTTGAAGGC[G/T]TACGGTGCTCTGACA | 4215 |
| rs777869698 | snp | C/G | 1.65102e-05 | 0.00287312 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691147 | TTGCTAAAGAACTTG[C/G]AGCATGAGCGCATCG | 4215 |
| rs777871160 | snp | C/G | 2.71028e-05 | 0.00368113 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691029 | AGGCCACTAACTAGG[C/G]CAAGCTGAGCTGAAC | 4215 |
| rs777960277 | snp | A/G | 1.7809e-05 | 0.00298398 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63681787 | AGAACCCTGGCCGAA[A/G]CTCACCTCCCCCTGG | 4215 |
| rs777970649 | snp | A/G | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694633 | GGTTGTGGCCTTTGC[A/G]CTCCTGGCCCAGCCT | 4215 |
| rs778030658 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63629299 | AGTTAATTTTTTTGT[A/G]TTTTTAGTAGAGACG | 4215 |
| rs778038580 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63630919 | CTTTATAGGCAACTT[C/T]GTCCTTTTCTGTACC | 4215 |
| rs778048510 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642884 | TGCCTCAGCTTTCCA[A/G]GTAGCTAAGACTACA | 4215 |
| rs778058231 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638534 | CAGTTATTCCTGTTG[A/C]TCCTGCTGAGTCCCT | 4215 |
| rs778072061 | snp | A/C | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686454 | ACCAGGGGAGTAAGA[A/C]GGCACAGGCAAGAGT | 4215 |
| rs778128052 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634612 | TAATCTTAACAAGAG[A/G]TACTAGATCTTTGGA | 4215 |
| rs778160285 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672608 | TGCACCCAGGCGAGA[A/G]TGCCTAAGCAGAGAC | 4215 |
| rs778214636 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635970 | GTTGTTTATTCAAGG[A/G]TGGAATGGGGCTGGC | 4215 |
| rs778218486 | snp | A/T | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63620924 | AGCAGGAGAATTGCT[A/T]GAACACGGGAGACGG | 4215 |
| rs778226984 | snp | C/T | 4.94719e-05 | 0.00497328 | intron-variant, missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63634779 | GCTCATGTGCAGGGG[C/T]CAGTGAGAAAAAGAA | 4215 |
| rs778266515 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685547 | AGCAGTGCAGAAAAT[A/T]CCTTGTCTGGAAGCT | 4215 |
| rs778322502 | snp | A/G | 1.83051e-05 | 0.00302527 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681944 | TGGCCTGTATCAGCA[A/G]ACCAAGCTCATAACA | 4215 |
| rs778340165 | snp | A/T | 1.65545e-05 | 0.00287697 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632654 | TGTATTTAAGTGTCT[A/T]AGTCCATGTGCTCTC | 4215 |
| rs778348455 | snp | A/C | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686538 | GGCTTTGGATTATCT[A/C]CTAAGCTTTGGAGGG | 4215 |
| rs778436310 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651087 | TTTTTAGTCATTTCT[A/G]TTCTAGAGTATTGGG | 4215 |
| rs778490728 | snp | A/G | 1.68026e-05 | 0.00289845 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634691 | AAATTATTAACCTCA[A/G]TTTTTTTGTTTTTAA | 4215 |
| rs778515351 | snp | C/G | 1.64885e-05 | 0.00287123 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691771 | GGCTTACGGTGCTCT[C/G]ACAGAGAGCGTGACC | 4215 |
| rs778517747 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63666959 | GTTCCTCTCCCCACT[C/T]TGGGGTGTCCAGACA | 4215 |
| rs778518266 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63642066 | TGGCTTATTATGGTC[A/T]ACCTGATGGGTGAAA | 4215 |
| rs778545287 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650534 | TCTTGAACTCCGGAC[C/G]TCAGGTGATCCACCC | 4215 |
| rs778598069 | snp | A/G | 1.67265e-05 | 0.00289188 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63652651 | CTACATTACATGAAC[A/G]ATGAGGTGAGAAGGC | 4215 |
| rs778602734 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690373 | TGAACTTGCTTCCAA[A/G]CAGGTCCAATTTGAT | 4215 |
| rs778607241 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63636440 | TGAATATTCTTAGAT[A/G]TGTGGCACATCCTAC | 4215 |
| rs778704633 | snp | A/G | 1.80667e-05 | 0.0030055 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652516 | TAAACCCTACGTTTT[A/G]AGTATACAATTAACC | 4215 |
| rs778715197 | snp | C/T | | | | | GRCh38.p7 | 17:63626631 | GAAGGATAAAAGTTT[C/T]TTATGAATTGAGGGT | 4215 |
| rs778736489 | snp | C/T | | | | | GRCh38.p7 | 17:63678390 | ATGGGCTGTTTGAGA[C/T]CATTGCAAAGGCATG | 4215 |
| rs778780995 | snp | C/T | 2.00898e-05 | 0.00316931 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689533 | CTCCTCTGGCCCTTG[C/T]ACCCTTTCAGGCAGA | 4215 |
| rs778796203 | snp | A/T | 1.67357e-05 | 0.00289268 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634705 | AGTTTTTTTGTTTTT[A/T]AAGAAAAAACACAAC | 4215 |
| rs778838516 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692840 | CCTTGGAAAGCTATT[A/G]TGGTGGGCTGAATAA | 4215 |
| rs778906951 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63640946 | GTACTGTCTCAGACA[C/T]CCCCCACTCCACTGC | 4215 |
| rs778923849 | in-del | -/CCCAGGACAGAAACCATGTAAGTA | 1.65957e-05 | 0.00288055 | cds-indel, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657890 | GGATATTGCTGTTGT[-/CCCAGGACAGAAACCATGTAAGTA]CCCAGGACAGAAACC | 4215 |
| rs778980840 | snp | C/T | 9.92162e-05 | 0.0070426 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688521 | TTTTCTTTTTGTTTT[C/T]TCCAGCCCATCCTTC | 4215 |
| rs779002300 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693100 | TGCAGGTGGCCTCTA[G/T]AACCCAGGAAAGGCA | 4215 |
| rs779021083 | snp | C/G | | | utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63695959 | AGTTGTGGGGCTTCA[C/G]GGTGACCTGGGCCCA | 4215 |
| rs779050615 | snp | C/T | 1.64958e-05 | 0.00287187 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688871 | TGTGCACCACAAGGA[C/T]TACAGTGATGGTGAG | 4215 |
| rs779071844 | snp | A/G | 1.65029e-05 | 0.00287248 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691155 | GAACTTGCAGCATGA[A/G]CGCATCGTGCAGTAC | 4215 |
| rs779076693 | snp | A/G | 1.64939e-05 | 0.0028717 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634804 | AAAGAAATTTTTGGT[A/G]AGGATCCAGATTACC | 4215 |
| rs779082692 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632438 | TGGAGGCTGCAGTGA[A/G]CTATGATCACGCCAC | 4215 |
| rs779097581 | snp | C/G | 1.80945e-05 | 0.00300781 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63681721 | GCTCCTCTTGGGCCA[C/G]ACACCCTGGGCTCTG | 4215 |
| rs779102571 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646734 | GTGGGAAGCCAAGGT[A/C]GAAGTTCTCAGTAGA | 4215 |
| rs779128848 | snp | A/C | | | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63694873 | CAGCCTCGCCCATCC[A/C]CTTGAGGTCTCAGCC | 4215 |
| rs779162078 | snp | A/G | 4.95094e-05 | 0.00497517 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691227 | CTTCATGGAGTACAT[A/G]CCAGGGGTACGTGCC | 4215 |
| rs779288956 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63644541 | CCATTTTAAATGAAT[A/G]AAGTAAATTTTCTCA | 4215 |
| rs779294650 | snp | C/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674233 | CATACTCCAACGCCT[C/G]AGTGGAGGCAATCAG | 4215 |
| rs779298975 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63659625 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCAATTC | 4215 |
| rs779300271 | in-del | -/AATG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63635313 | TTGTGATAAGCTAAT[-/AATG]GGAATCCTACCTAAG | 4215 |
| rs779301433 | snp | C/G/T | 4.95719e-05 | 0.00497834 | missense, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693644 | AGATTGCCACCCAGC[C/G/T]CACCAATCCTCAGCT | 4215 |
| rs779312742 | in-del | -/TGGATTGAAAA | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63673175 | AATTCTTCTTTATTT[-/TGGATTGAAAA]TCAGCTTTCTCTCAC | 4215 |
| rs779324350 | snp | A/G | 1.68371e-05 | 0.00290143 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646020 | TCTAACCTGTCTATC[A/G]TTCTTTTTGGCAGAG | 4215 |
| rs779389261 | snp | C/T | 1.65499e-05 | 0.00287657 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63692306 | TGGGGCCAGCAAACG[C/T]CTGCAGACGATCTGT | 4215 |
| rs779550461 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637942 | GGCAGGGCCTTGGCT[A/G]TCATTTCTAGAGGAA | 4215 |
| rs779561149 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63638163 | GCTTTATAATCGTCT[C/G]TTCCACTGATCTCCT | 4215 |
| rs779593198 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634206 | ACTTTTCGAAGGAGC[A/G]TTTTACCAGAAGTGA | 4215 |
| rs779596121 | in-del | -/AA | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63683752 | AAGTGAAAATATGAT[-/AA]GTTTTGTTTTTTCTT | 4215 |
| rs779647468 | snp | A/C | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63622158 | CTAGACAGCCCTCGG[A/C]AACCGCCTTGGCTTC | 4215 |
| rs779667463 | snp | A/T | 1.67576e-05 | 0.00289457 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688932 | TCAAGAAAGGACAAG[A/T]TGCCATGGGGAGGGT | 4215 |
| rs779675651 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689407 | ATGGGCTGGAGCTGG[C/T]ATTATCTATCACTTC | 4215 |
| rs779681140 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652877 | TCCCCCTACTCATTC[A/G]GTGCAGATAGCTCTA | 4215 |
| rs779822053 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627308 | TCTTAATCTCTAAAA[C/T]TAACCTCTTTCTCCT | 4215 |
| rs779869293 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666182 | ATTGCTGACCCTCCT[C/T]TCAGGCCCTTGACCT | 4215 |
| rs779871798 | snp | C/T | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63686857 | CTTTCATCTTCCCTT[C/T]ACGGGATCTGGGAAA | 4215 |
| rs780043336 | in-del | -/TGCC | 1.81969e-05 | 0.00301631 | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63681923 | AGGGGGGCTGGGATA[-/TGCC]TGTGGCCTGTATCAG | 4215 |
| rs780054938 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634128 | TTCTTACACTATTTT[A/C]ATATGTTATTCAGTC | 4215 |
| rs780110719 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631454 | TGGAATCTTTTGTAT[G/T]TGCTTCTTTTAAGGT | 4215 |
| rs780121129 | snp | A/C/G | 6.61512e-05 | 0.00575083 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691738 | TGGCCTCCAGGGCTC[A/C/G]GTGAAAGACCAGTTG | 4215 |
| rs780177464 | snp | G/T | | | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691559 | GCTCTGCTTGAGAAG[G/T]ACTTGGGGTACTCTC | 4215 |
| rs780211229 | snp | A/G | 1.71873e-05 | 0.00293144 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652678 | AGGCAGATGGATGGG[A/G]CAGGGACAAGAGGGG | 4215 |
| rs780212319 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63667038 | CCAGCCCCCCGAGCC[C/T]AGAAGCAGGCACCTC | 4215 |
| rs780230406 | snp | C/T | 3.30568e-05 | 0.00406538 | synonymous-codon, utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693654 | CCAGCCCACCAATCC[C/T]CAGCTGCCCTCCCAC | 4215 |
| rs780240107 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669223 | GGACCTTGAAAGATT[A/G]TGGAGGATTTCCACA | 4215 |
| rs780261226 | in-del | -/TTTG | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658749 | CTTTTTTTTTTTTTT[-/TTTG]AGACAGAGTTTTGCT | 4215 |
| rs780317452 | snp | A/G | 1.65091e-05 | 0.00287303 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63634837 | TTAAAGCCAAAATGT[A/G]CTTTTAAATCTGCTA | 4215 |
| rs780323692 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63688753 | GTGGCTCACATTGAC[C/T]TACCCAGAAGCCAGT | 4215 |
| rs780332184 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655597 | CTGGGTTCAAGTGAT[C/T]CCCCCACCTCAGTTT | 4215 |
| rs780350389 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646933 | ATTGATATACTACCC[C/G]CTGCCACCCTCAGCT | 4215 |
| rs780354876 | in-del | -/CCAT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624385 | TTAAGGGTATGTAGA[-/CCAT]CCATCCACTTCCTAC | 4215 |
| rs780415686 | snp | A/G | 1.65329e-05 | 0.0028751 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632664 | TGTCTTAGTCCATGT[A/G]CTCTCTTTCATTGCA | 4215 |
| rs780428671 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660111 | GGTCTTCATCACCTC[C/T]GCTGATACTGTCAGT | 4215 |
| rs780436582 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667967 | TATTACTTGTTAACC[C/T]AGGATTCCTGTGGAT | 4215 |
| rs780441933 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631586 | CCAAATGCTATTTGA[A/G]TGGGCAAAGATCTCT | 4215 |
| rs780502633 | snp | C/T | 5.24581e-05 | 0.00512116 | missense, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689678 | CCCCGTGGGCGCCTG[C/T]GGAGTGCGGACAGCG | 4215 |
| rs780533514 | snp | C/T | | | intron-variant, downstream-variant-500B | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682192 | CCTACAGGCAGGCAC[C/T]ACCACGCCCAGCTCA | 4215 |
| rs780588217 | snp | A/C | 1.65515e-05 | 0.00287671 | missense, nc-transcript-variant | MAP3K3 | GRCh38.p7 | 17:63657822 | TGAAAAACCAAGATG[A/C]TCTTGATAAAGCAAT | 4215 |
| rs780677885 | snp | C/T | 1.68221e-05 | 0.00290014 | utr-variant-3-prime | MAP3K3 | GRCh38.p7 | 17:63693788 | ACTGAGCTCTCACGG[C/T]CACACAGCTGCCGGT | 4215 |
| rs780684814 | snp | C/G | 1.74616e-05 | 0.00295474 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63652685 | TGGATGGGGCAGGGA[C/G]AAGAGGGGCAGATGC | 4215 |
| rs780686755 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63624575 | CTATATAGGCTGGGT[C/T]TAGAGCCCCAAAGAA | 4215 |
| rs780790306 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63623429 | TTCACATCCTACTTT[G/T]TGAAAAATCCCGTTG | 4215 |
| rs780804688 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660262 | CTGGAGTGCAGTGGC[A/G]CAGTGACAGCTCACC | 4215 |
| rs780804774 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63667622 | CCAAGGTCTGTGGAT[A/G]CTCAAGTCCCTGAAA | 4215 |
| rs780812524 | snp | C/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63675819 | TGACCCCTGCCTATG[C/T]AGCCTTCTGAGACCT | 4215 |
| rs780840851 | snp | A/T | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63677225 | AGTGGCAAAGCCTGA[A/T]CTGAACCCACGTATA | 4215 |
| rs780913663 | snp | A/G | 0.000198595 | 0.00996283 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691033 | CACTAACTAGGGCAA[A/G]CTGAGCTGAACCCAG | 4215 |
| rs780958866 | snp | A/G | 1.80218e-05 | 0.00300176 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63689569 | ATTTCCCCGAATACG[A/G]CGTCATCAAGGCAAC | 4215 |
| rs781002395 | snp | A/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654078 | TTCACCATGTTGCCC[A/T]GGCTGGTCTCAAATT | 4215 |
| rs781003567 | snp | C/T | 1.65258e-05 | 0.00287448 | intron-variant, upstream-variant-2KB | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691254 | TGCCCCTTGAATGCA[C/T]GTGAGACACACACAA | 4215 |
| rs781019559 | in-del | -/G | | | upstream-variant-2KB | MAP3K3 | GRCh38.p7 | 17:63621686 | AGCAGCGTCGGGACC[-/G]GAGGACCAGTCGGGG | 4215 |
| rs781087212 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63656681 | TTTGCATCTTATGAA[G/T]CTCTTAATACCAAGT | 4215 |
| rs781107315 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63693004 | CAGAAGGGTCTCAAG[A/G]GGTCAGAGTGGCTAA | 4215 |
| rs781191575 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664108 | AAAAAATAGCCGGGC[A/G]TGGTAGCGGGCGCCT | 4215 |
| rs781198336 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63666359 | CATATATAAGCTGGG[C/T]ATGGTAGCATGTACC | 4215 |
| rs781252416 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63631023 | CAGGCACGGTGGCTT[A/G]TGTCTGTAATCCCAG | 4215 |
| rs781268190 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63661248 | GATGGGGTTTCGCAC[C/T]GTTGGCGAGGCTAGT | 4215 |
| rs781351650 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63633058 | CATGGTGAAACCCTG[C/T]CCCTACTAAAAAACA | 4215 |
| rs781353756 | snp | A/G | 1.64963e-05 | 0.00287192 | intron-variant | MAP3K3 | GRCh38.p7 | 17:63632823 | TGTGACCCTGGCAGA[A/G]CTAAGTGAGATTTGT | 4215 |
| rs781384783 | snp | C/T | 1.65334e-05 | 0.00287514 | synonymous-codon, intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63690397 | ATTTGATCCAGACAG[C/T]CCTGAGACAAGCAAG | 4215 |
| rs781485409 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63655951 | TGTACTGTTTTTGGC[A/G]AGGCGCGATGGTTCA | 4215 |
| rs781543643 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63648504 | TATCACTGCTTGGGA[C/G]AGTTGATTTGGAAGA | 4215 |
| rs781559314 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650327 | TTTTTTGAGACAGAG[G/T]CTCTTGCTCTGTTGC | 4215 |
| rs781592340 | snp | A/C | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63685330 | TTTTCTCCCTCCTGG[A/C]AACTTGCCTTTCAAA | 4215 |
| rs781608936 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | MAP3K3, LIMD2 | GRCh38.p7 | 17:63696445 | AAGTAGAGGGGTCCT[A/G]GGGTGATCTGGCTGA | 4215 |
| rs781616738 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63654772 | TAGGTGCAGTGACTC[-/A]ACGCCTGTTAATCCC | 4215 |
| rs781662159 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63669291 | GTCTGTGGAGAGCTC[G/T]CTATTCTTCAGGTCC | 4215 |
| rs781759438 | snp | C/T | 0.000158525 | 0.00890153 | intron-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63691007 | GTTCCCAAGGCAGAT[C/T]CCTGTGAGGCCACTA | 4215 |
| rs796095540 | multinucleotide-polymorphism | CGG/GGA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63662856 | GAGATGGGGTTGGGC[CGG/GGA]GGGCGGTCCTCACCA | 4215 |
| rs796143086 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63627280 | TACTCCTCCTTTTCC[C/T]AGATTCTTAACCTCT | 4215 |
| rs796191998 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63660372 | CATGCTTGGCTTTTC[-/T]TTTTTTTTTTTTTAA | 4215 |
| rs796198524 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625289 | AATAATAGGAAATTT[G/T]TTTTTTTGCTTTGAT | 4215 |
| rs796230944 | snp | A/G | | | intron-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63674633 | TGAGATTATAGGTAT[A/G]AGCCACCATGCCCAG | 4215 |
| rs796285295 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63665697 | GTTTCCTTTTTGACC[C/G]TTAGCAGAGAGCTAT | 4215 |
| rs796333785 | snp | A/C | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63646462 | GTGCCATTACTATTC[A/C]CAGTAGAGCAGCCCT | 4215 |
| rs796433141 | in-del | -/A | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664086 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAATAG | 4215 |
| rs796460534 | in-del | -/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651430 | GTGAGCCGTTATCAT[-/T]GCCACTGCACTCCAG | 4215 |
| rs796514153 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63639077 | CCCCAGGAATCATGC[A/G]GTCTTACTGGGAAGT | 4215 |
| rs796566770 | snp | C/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63664244 | AGAGCGAGACTCCGT[C/T]TCAAAAAAAAAAAAA | 4215 |
| rs796579581 | snp | A/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63625577 | TTGTGACTTACAGAC[A/G]CCTTGTCTAGGGTTC | 4215 |
| rs796649852 | snp | C/G | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63651860 | TCTGTAGTAGAAAAT[C/G]TTAATTCTGAGGAAA | 4215 |
| rs796715308 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K3, LOC107984984 | GRCh38.p7 | 17:63672406 | TAAGACAGGAATACT[A/G]GAAGAGAGCCTGGTT | 4215 |
| rs796718858 | snp | G/T | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637880 | GATGTTCATGAGTGG[G/T]TGCTTCAGAACAGAA | 4215 |
| rs796763736 | snp | A/G | | | intron-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63687910 | ACAGCACTCCAGCCC[A/G]GCAGCAGAGCGAGAC | 4215 |
| rs796794982 | in-del | -/T | | | intron-variant, nc-transcript-variant | MAP3K3, LOC101927898 | GRCh38.p7 | 17:63682603 | AGAATTCAGTTTTTT[-/T]GTGGCTGTAGGACTG | 4215 |
| rs796796374 | in-del | -/AAAAAAA | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63637193 | AAACTGAGACCAACC[-/AAAAAAA]AAAAAAAAAAAAGAG | 4215 |
| rs796809498 | multinucleotide-polymorphism | AG/TT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650695 | AGAGAGAGAGAGAGA[AG/TT]TTTTTTTTTTTTTAG | 4215 |
| rs796848672 | in-del | -/TTTT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63658748 | TCTTTTTTTTTTTTT[-/TTTT]GAGACAGAGTTTTGC | 4215 |
| rs796986437 | in-del | -/AGT | | | intron-variant | MAP3K3 | GRCh38.p7 | 17:63650695 | GAGAGAGAGAGAGAG[-/AGT]TTTTTTTTTTTTTAG | 4215 |