SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs280621 | snp | C/T | 0.177824 | 0.239355 | utr-variant-3-prime, nc-transcript-variant | BARD1 | GRCh38.p7 | 2:214725858 | GTGACTGTAATGAGG[C/T]CCATGAACGTTTAGA | 580 |
rs280622 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | BARD1 | GRCh38.p7 | 2:214725686 | TTCAGTTTGATGTGC[A/G]TATCTTTGAAAAGGG | 580 |
rs280623 | snp | C/T | 0.0655868 | 0.168795 | downstream-variant-500B | BARD1 | GRCh38.p7 | 2:214725321 | TCAGGTGAAATGAAC[C/T]GTATTCCCCCCCTTT | 580 |
rs723904 | snp | C/T | 0.419456 | 0.183806 | intron-variant | BARD1 | GRCh38.p7 | 2:214764182 | ATACTTTTTCCTCTT[C/T]TTTGATAAAAGGTCA | 580 |
rs723905 | snp | A/G | 0.497502 | 0.035255 | intron-variant | BARD1 | GRCh38.p7 | 2:214764036 | GGCAGCTTTTGCCCA[A/G]TTGGCATCCATGGCA | 580 |
rs748867 | snp | G/T | 0.107694 | 0.205546 | intron-variant | BARD1 | GRCh38.p7 | 2:214736304 | TTCCTGATGGTTTTT[G/T]ATTTGATTTTTAATA | 580 |
rs748868 | snp | A/G | 0.107694 | 0.205546 | intron-variant | BARD1 | GRCh38.p7 | 2:214736283 | ATTTTTAATATAGAA[A/G]CAATATATGACATAA | 580 |
rs748869 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | BARD1 | GRCh38.p7 | 2:214736078 | TGTAAACAATTTTCA[A/G]AGCACATTTATGATA | 580 |
rs895458 | snp | A/G | 0.225301 | 0.248777 | intron-variant | BARD1 | GRCh38.p7 | 2:214736043 | AAAATTATAAGATTC[A/G]GAAATTCAGCTTAGC | 580 |
rs895459 | snp | C/T | 0.478354 | 0.101757 | intron-variant | BARD1 | GRCh38.p7 | 2:214735533 | ATTGGAAGTAATAAA[C/T]AGTAAATCCTCATTG | 580 |
rs895460 | snp | C/T | 0 | 0 | intron-variant | BARD1 | GRCh38.p7 | 2:214765950 | GCAGGGCTTCTAGGT[C/T]GTAATTTTTTATTGG | 580 |
rs1048108 | snp | C/T | 0.492233 | 0.0618321 | BARD1, LOC101928103 | 2 | allele_origin=T(germline)/C(germline) | 2:214809500 | GAGCCTCGTTCCGCG[C/T]CCGCCATGGAACCGG | 580 |
rs1048171 | snp | C/G | 0.478354 | 0.101757 | utr-variant-3-prime, nc-transcript-variant | BARD1 | GRCh38.p7 | 2:214725885 | TCAGTGTGGAAAATG[C/G]ATTAATCATATTCTA | 580 |
rs1129804 | snp | C/G | 0.414111 | 0.188594 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | BARD1, LOC101928103 | GRCh38.p7 | 2:214809599 | CTTGCTTCCCGCTCT[C/G]CGAGGAGCCTTTCAT | 580 |
rs1374230 | snp | C/T | 0.437118 | 0.165792 | intron-variant | BARD1 | GRCh38.p7 | 2:214754055 | AAGTATCAAGAATAG[C/T]GGATGAGTTTCTTTT | 580 |
rs1374231 | snp | C/T | 0.128632 | 0.218563 | intron-variant | BARD1 | GRCh38.p7 | 2:214733358 | TTTATCTGTATAAAG[C/T]GTATATGAAACATAA | 580 |
rs1374232 | snp | A/T | 0.227369 | 0.248974 | intron-variant, downstream-variant-500B | BARD1 | GRCh38.p7 | 2:214738614 | TTTTATTATAGGAAA[A/T]GTAAGCTTAATATAA | 580 |
rs1446365 | snp | C/G | 0.489083 | 0.0730708 | intron-variant | BARD1 | GRCh38.p7 | 2:214748718 | AGAGAAATTCAAACC[C/G]CTTCCTTTAGGGAAG | 580 |
rs1446366 | snp | A/T | 0.49889 | 0.0235361 | intron-variant | BARD1 | GRCh38.p7 | 2:214743132 | CTAGTCACAGCCTCT[A/T]AGCTGGATCAGACTG | 580 |
rs1446367 | snp | A/T | 0.49889 | 0.0235361 | intron-variant | BARD1 | GRCh38.p7 | 2:214743254 | AACCAAATCAACTTC[A/T]AACTACAGATTAAAT | 580 |
rs1542173 | snp | A/G | 0.399253 | 0.200558 | intron-variant | BARD1 | GRCh38.p7 | 2:214792836 | TCCCAAAACAAAACA[A/G]AAGGTCTTTCCCAGT | 580 |
rs1550841 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | BARD1 | GRCh38.p7 | 2:214726060 | AAAAAAGGTGGGGGG[A/C]CCGATGAAATAAAGG | 580 |
rs1550843 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BARD1 | GRCh38.p7 | 2:214758439 | CATAACTTATTTTGT[G/T]CCCTTATCTTCATTC | 580 |
rs1838800 | snp | C/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | BARD1 | GRCh38.p7 | 2:214726875 | AATGAATGACAAAAA[C/G]TAAGAGACCTCATAG | 580 |
rs1838801 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | BARD1 | GRCh38.p7 | 2:214787699 | ACATGCATCTCTGTT[A/C]CTCAATATTTTGTGA | 580 |
rs1838802 | snp | A/G | 0.49889 | 0.0235361 | intron-variant | BARD1 | GRCh38.p7 | 2:214743172 | AGACAAGCATCACAA[A/G]AAAAGAAGTGGTAGC | 580 |
rs1838803 | snp | A/T | 0.0792508 | 0.182605 | intron-variant | BARD1 | GRCh38.p7 | 2:214746016 | GAACCTTTTAAATAA[A/T]TTTTTTCTCTTTATT | 580 |
rs1838804 | snp | C/T | 0.404035 | 0.196909 | intron-variant | BARD1 | GRCh38.p7 | 2:214746053 | TCAAGAAAATGTCAA[C/T]TGTGATAGCTCTCTA | 580 |
rs1867795 | snp | G/T | 0.480382 | 0.097079 | intron-variant | BARD1 | GRCh38.p7 | 2:214736905 | GCAAATTGTTGCTTG[G/T]AGTAAAAGCATATTA | 580 |
rs1867796 | snp | A/C | 0.490782 | 0.0672626 | intron-variant | BARD1 | GRCh38.p7 | 2:214740992 | AGTATCCATTTAAAG[A/C]AGCCAACTTGTTAGA | 580 |
rs1900243 | snp | G/T | 0.0425829 | 0.139564 | | | GRCh38.p7 | 2:214782662 | TAAAGTAGCAGGTGA[G/T]TGTAAAGAAGAGTAT | 580 |
rs1972957 | snp | A/G | 0.493881 | 0.054972 | intron-variant | BARD1 | GRCh38.p7 | 2:214758360 | GTTATTGAGCTGTTC[A/G]TATATGCTAGGTACT | 580 |
rs1972958 | snp | A/G | 0.493793 | 0.055364 | intron-variant | BARD1 | GRCh38.p7 | 2:214758231 | GGATTTAAGTAATTC[A/G]TGTAAAGTCATAAGA | 580 |
rs1979028 | snp | A/T | 0.449091 | 0.151204 | utr-variant-3-prime, nc-transcript-variant | BARD1 | GRCh38.p7 | 2:214728182 | ATAGGATAAAGACAA[A/T]TGCAGATAGGAGAAT | 580 |
rs2034250 | snp | A/T | 0.418169 | 0.184985 | intron-variant, downstream-variant-500B | BARD1 | GRCh38.p7 | 2:214739080 | CTCTTTGCAGCCATG[A/T]ACTCCTGGGTTCAAG | 580 |
rs2034251 | snp | A/G | 0.48666 | 0.0805725 | intron-variant | BARD1 | GRCh38.p7 | 2:214762228 | TCATAAACATTTTAT[A/G]CACATAGCCTGAAGG | 580 |
rs2034252 | snp | A/G | 0 | 0 | intron-variant | BARD1 | GRCh38.p7 | 2:214742002 | TACAAATAAAATTCT[A/G]CTTGAATCTATTTGG | 580 |
rs2053710 | snp | A/G | 0.499187 | 0.0201513 | intron-variant | BARD1 | GRCh38.p7 | 2:214751984 | ctgatttgaattgaa[A/G]cctgaatgttgaagt | 580 |
rs2070093 | snp | C/T | 0.303537 | 0.2442 | BARD1 | 2 | allele_origin=T(germline)/C(germline) | 2:214767532 | AGCCAAGAATGGGCA[C/T]GTGGATATAGTCAAG | 580 |
rs2070094 | snp | A/G | 0.470394 | 0.118011 | BARD1 | 2 | allele_origin=G(germline)/A(germline) | 2:214767531 | GCCAAGAATGGGCAT[A/G]TGGATATAGTCAAGC | 580 |
rs2070096 | snp | C/G | 0.326122 | 0.238129 | BARD1 | 2 | allele_origin=G(germline)/T(germline)/C(germline) | 2:214780821 | TTTTGTTAAGCAAAC[C/G]GTGCCCTCAGAAAAT | 580 |
rs2075621 | snp | A/G | 0.40386 | 0.197046 | intron-variant | BARD1 | GRCh38.p7 | 2:214752776 | TGTGAAAAATTCATA[A/G]TACTATATTCAGTAA | 580 |
rs2075622 | snp | A/C | 0.480853 | 0.0959518 | intron-variant | BARD1 | GRCh38.p7 | 2:214729147 | AAACCCAAAAAATTT[A/C]TGAATCTGAAATGCT | 580 |
rs2075623 | snp | C/G | 0.480931 | 0.0957637 | intron-variant | BARD1 | GRCh38.p7 | 2:214729127 | TCTGAAATGCTTCTC[C/G]TCCAAATGTTTCAGG | 580 |
rs2121284 | snp | A/G | 0.435407 | 0.167703 | intron-variant | BARD1 | GRCh38.p7 | 2:214791536 | TTAACTGTGGAAAGA[A/G]AGTAAAATGTTTTGT | 580 |
rs2121285 | snp | C/G | 0.401392 | 0.198948 | intron-variant | BARD1 | GRCh38.p7 | 2:214791444 | TGTTTGTAGAAGAAC[C/G]TGTTCTTGACTGGCA | 580 |
rs2228455 | snp | C/T | 0.00989172 | 0.0696277 | missense, nc-transcript-variant | BARD1 | GRCh38.p7 | 2:214730455 | GAAGAAAAGTATGAA[C/T]TTCCTGAAGGTCCAY | 580 |
rs2228456 | snp | C/T | 0.0127095 | 0.0786971 | BARD1 | 2 | allele_origin=T(germline)/C(germline) | 2:214730479 | CTACGAAGAAAAGTA[C/T]GTGAACAGGAAGAAA | 580 |
rs2229571 | snp | C/G | 0.495257 | 0.0484641 | BARD1 | 2 | allele_origin=G(germline)/C(germline) | 2:214780740 | TGGTACATCAGGGAG[C/G]AAAAACAGTAACATG | 580 |
rs2292821 | snp | A/T | 0.404559 | 0.196498 | utr-variant-3-prime, nc-transcript-variant | BARD1 | GRCh38.p7 | 2:214726065 | AGGTGGGGGGACCGA[A/T]GAAATAAAGGAAAAA | 580 |
rs2734673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BARD1 | GRCh38.p7 | 2:214796680 | CCTAAGGCTGCCATA[A/G]CAAAGAACCAAAAAC | 580 |
rs2734674 | snp | C/T | 0.39527 | 0.203462 | intron-variant | BARD1 | GRCh38.p7 | 2:214794171 | ctcaacttcttggct[C/T]gggtgatcatccaat | 580 |
rs2734675 | snp | A/G | 0.39527 | 0.203462 | intron-variant | BARD1 | GRCh38.p7 | 2:214794123 | tgagactacaggtgc[A/G]ccccaccacgcctgg | 580 |
rs2888294 | snp | C/G | 0.499137 | 0.0207489 | intron-variant | BARD1 | GRCh38.p7 | 2:214749504 | CCATGTAATAAAAAC[C/G]CTCCTTTTCTGAAAG | 580 |
rs3046934 | in-del | -/TACT | | | intron-variant | BARD1 | GRCh38.p7 | 2:214748880 | CATTCAGCACACACT[-/TACT]GAACACTCAGTATGT | 580 |
rs3046935 | in-del | -/AAAA | 0.0162398 | 0.0886349 | intron-variant | BARD1 | GRCh38.p7 | 2:214729976 | ATGCTCGTTGGAAAT[-/AAAA]AAAGTTTCATAATTC | 580 |
rs3738885 | snp | A/C/G | 0.00043619 | 0.0147616 | BARD1 | 2 | allele_origin=G(germline)/A(germline)/C(germline) | 2:214781152 | AGCAAAAGCTGGTAT[A/C/G]CTTCTGTAGCCAACC | 580 |
rs3738886 | snp | G/T | 0.44651 | 0.154543 | intron-variant | BARD1 | GRCh38.p7 | 2:214730721 | GCTTAATCCTCCAAA[G/T]AAAGAGTTTTTTAAA | 580 |
rs3738887 | snp | A/T | 0.476918 | 0.104919 | intron-variant | BARD1 | GRCh38.p7 | 2:214730716 | ATCCTCCAAAGAAAG[A/T]GTTTTTTAAAATATT | 580 |
rs3738888 | snp | C/T | 0.015744 | 0.0873161 | BARD1 | 2 | allele_origin=T(germline)/C(germline) | 2:214730440 | ATTCCTGAAGGTCCA[C/T]GCAGAAGCAGGCTCA | 580 |
rs3754546 | snp | C/T | 0.322483 | 0.239262 | intron-variant | BARD1 | GRCh38.p7 | 2:214792971 | AAATTAGAAAAACTC[C/T]TCTAACTCTGAAACT | 580 |
rs3754548 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | BARD1 | GRCh38.p7 | 2:214787694 | CATCTCTGTTCCTCA[A/G]TATTTTGTGATGTAC | 580 |
rs3768704 | snp | A/G | 0.32627 | 0.238082 | intron-variant | BARD1 | GRCh38.p7 | 2:214791195 | CAGCTAGTTATCTGC[A/G]TCATTGTATTCAACT | 580 |
rs3768705 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | BARD1 | GRCh38.p7 | 2:214786226 | TTGTATCTCTTAAGT[A/G]TTAAAAGTTCTCAGT | 580 |
rs3768707 | snp | C/T | 0.400325 | 0.199756 | intron-variant | BARD1 | GRCh38.p7 | 2:214780411 | GAGAAGCCAGATTCA[C/T]AGGGAGAGCATCTCT | 580 |
rs3768708 | snp | A/G | 0.417359 | 0.185718 | intron-variant | BARD1 | GRCh38.p7 | 2:214780322 | ATATTTGAATATTTC[A/G]GCTTTTATTTTGCCA | 580 |
rs3768709 | snp | A/G | 0.283158 | 0.247791 | intron-variant | BARD1 | GRCh38.p7 | 2:214780306 | GCTTTTATTTTGCCA[A/G]GTGCTTTTGCTTTTG | 580 |
rs3768710 | snp | A/G | 0.284209 | 0.247648 | intron-variant | BARD1 | GRCh38.p7 | 2:214777512 | TATTGTTTCTTAAGC[A/G]TGTTGGTAAACTTGC | 580 |
rs3768711 | snp | A/G | 0.324382 | 0.238678 | intron-variant | BARD1 | GRCh38.p7 | 2:214776388 | GAAACTAAGATACTC[A/G]TTGTTTATTCTTCTG | 580 |
rs3768712 | snp | A/C | 0.367503 | 0.220665 | intron-variant | BARD1 | GRCh38.p7 | 2:214772871 | AAAGAAGCCAGAATC[A/C]AAACTTAATTTATTT | 580 |
rs3768713 | snp | C/T | 0.307919 | 0.243198 | intron-variant | BARD1 | GRCh38.p7 | 2:214772781 | ATAATTTTATTTATG[C/T]GCATGACATTACATT | 580 |
rs3768714 | snp | C/T | 0.496842 | 0.0396107 | intron-variant | BARD1 | GRCh38.p7 | 2:214772595 | GACATGAAAGAAAAA[C/T]AGCAACTGTCTAACA | 580 |
rs3768715 | snp | A/G | 0.367297 | 0.220775 | intron-variant | BARD1 | GRCh38.p7 | 2:214772579 | AGCAACTGTCTAACA[A/G]CCTTAAAAGAGAGTC | 580 |
rs3768716 | snp | A/G | 0.260504 | 0.249779 | intron-variant | BARD1 | GRCh38.p7 | 2:214771070 | CATCCCGCTGCATAA[A/G]TGCCTCCTTCTTCCT | 580 |
rs3820726 | snp | C/T | 0.367503 | 0.220665 | intron-variant | BARD1 | GRCh38.p7 | 2:214773032 | GCCTTCAGTGTATTA[C/T]TTGAAAATACCAAAT | 580 |
rs3820727 | snp | G/T | 0.450859 | 0.148847 | intron-variant | BARD1 | GRCh38.p7 | 2:214770269 | TTCGTATAGTTGAAT[G/T]AGTTGATAATGGGTG | 580 |
rs3835755 | in-del | -/A | 0 | 0 | intron-variant | BARD1 | GRCh38.p7 | 2:214788186 | GGTGTTGGTGACATT[-/A]AAAAAAAAAATACTT | 580 |
rs3856564 | snp | C/G | 0.228547 | 0.249078 | intron-variant | BARD1 | GRCh38.p7 | 2:214732447 | GTCACCCAGGTTGGG[C/G]CGCAGTGGCGCAATC | 580 |
rs3948124 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | BARD1 | GRCh38.p7 | 2:214785658 | AGATAGAGTGCCAGA[C/T]TGGGAGTTAGGGGAC | 580 |
rs3953393 | snp | A/G | | | intron-variant | BARD1 | GRCh38.p7 | 2:214803019 | accgggttgggggta[A/G]ggtcatagattaaca | 580 |
rs4016112 | snp | C/G | 0.345037 | 0.231231 | intron-variant | BARD1 | GRCh38.p7 | 2:214803032 | tgtttcagagagcac[C/G]gggttgggggtaggg | 580 |
rs4088306 | snp | C/T | 0 | 0 | intron-variant | BARD1 | GRCh38.p7 | 2:214776187 | TTAAAATGGCAATGA[C/T]TACTCATAATTTATG | 580 |
rs4234005 | snp | C/T | 0.463666 | 0.129795 | intron-variant | BARD1 | GRCh38.p7 | 2:214768687 | CCAATTGTTTCCAAG[C/T]ATTTGTGTCATTCTG | 580 |
rs4234006 | snp | A/G | 0.353587 | 0.22753 | intron-variant | BARD1 | GRCh38.p7 | 2:214768739 | TTTTTTAGTAATAAT[A/G]AGCAAAGACCTTTAA | 580 |
rs4234007 | snp | C/T | 0.464096 | 0.129085 | intron-variant | BARD1 | GRCh38.p7 | 2:214768762 | ACCTTTAAAAATGTT[C/T]AATGTAAGCAAAGAT | 580 |
rs4423591 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | BARD1 | GRCh38.p7 | 2:214768643 | TGCATTCAAATCTCA[C/T]GTTTGTCCTAATGTA | 580 |
rs4672728 | snp | A/T | 0.49917 | 0.0203505 | intron-variant | BARD1 | GRCh38.p7 | 2:214750657 | CAAAGACTGACCCTA[A/T]CCTCCAGCCCCAGGA | 580 |
rs4672729 | snp | A/G | 0.492533 | 0.0606443 | intron-variant | BARD1 | GRCh38.p7 | 2:214778759 | TGCAAAGCTGAAAAC[A/G]TTTACTCTAACTGCA | 580 |
rs4673893 | snp | A/G | 0.419776 | 0.18351 | intron-variant | BARD1 | GRCh38.p7 | 2:214763653 | TCTTACCCTTCTTCC[A/G]TGGGAAGAGTTCAGG | 580 |
rs4673894 | snp | C/T | 0.48679 | 0.0801892 | intron-variant | BARD1 | GRCh38.p7 | 2:214763665 | TCCATGGGAAGAGTT[C/T]AGGCCTGGTTATTGA | 580 |
rs4673895 | snp | C/T | 0.487933 | 0.0767327 | intron-variant | BARD1 | GRCh38.p7 | 2:214763774 | TTGAGATGTTAATGG[C/T]TTATAAGGAGTAAGA | 580 |
rs4673896 | snp | A/C | 0.486725 | 0.0803809 | intron-variant | BARD1 | GRCh38.p7 | 2:214763937 | ATTCTAGAAGACAGT[A/C]TCTAGAACATTGAGA | 580 |
rs4673897 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | BARD1 | GRCh38.p7 | 2:214771192 | TACCTAAGTCCATGA[A/C]GATAAAGCAAAAATA | 580 |
rs4673898 | snp | A/C | 0.0836354 | 0.186609 | intron-variant | BARD1 | GRCh38.p7 | 2:214778774 | ATTTACTCTAACTGC[A/C]CCTTTAAGAAAGAAC | 580 |
rs4673899 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | BARD1 | GRCh38.p7 | 2:214778987 | ACACTAGCTACTTAT[A/G]TCTATAACTTTGTTT | 580 |
rs4673900 | snp | A/T | 0.0836354 | 0.186609 | intron-variant | BARD1 | GRCh38.p7 | 2:214788075 | TCCTCTATTATAAAA[A/T]AGTCATAGCATATAT | 580 |
rs4673901 | snp | C/G | 0.0836354 | 0.186609 | intron-variant | BARD1 | GRCh38.p7 | 2:214788152 | GCAGAAAATAGAAAA[C/G]GAAATTGTAATACTA | 580 |
rs4673902 | snp | A/C | 0.0836354 | 0.186609 | intron-variant | BARD1 | GRCh38.p7 | 2:214793610 | CTCATCAAGAACTAC[A/C]ACCTCATTTTTGGAT | 580 |
rs4986840 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | BARD1 | GRCh38.p7 | 2:214730575 | TAGGTAAATTGCTTG[A/G]TTTTAATGAGAGAGA | 580 |
rs4986842 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BARD1 | GRCh38.p7 | 2:214745914 | AAGTAACAGTCTGTT[C/T]AATGTCTTTGTCTAG | 580 |