SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs346461076	snp	A/G			intron-variant	?	TAIR10	2:16890226	GAAAAAATTGGAAAG[A/G]CTCGTAATCTCAACT	818638
rs346468034	snp	C/T			intron-variant	?	TAIR10	2:16890476	CACTTATAGGTGGGC[C/T]AGTGGTAGGAAGGAT	818638
rs346496513	snp	C/T			intron-variant	?	TAIR10	2:16890617	AACTACTCTTGCCGC[C/T]TTCGGGACGCACGCA	818638
rs346550902	snp	G/T			intron-variant	?	TAIR10	2:16890189	TTAATCATTTATTTA[G/T]TTACGGAATTATTTT	818638
rs346624589	snp	A/G			intron-variant	?	TAIR10	2:16890489	GCCAGTGGTAGGAAG[A/G]ATTTCGGGCTGAGGG	818638
rs346650898	snp	G/T			missense	?	TAIR10	2:16890930	GAAAGCCTCTAATTC[G/T]TCGTGTTTCATCTCA	818638
rs346651977	snp	G/T			intron-variant	?	TAIR10	2:16889786	CCAAATTGGCAGTGG[G/T]TGAATCTAATTACTC	818638
rs346675427	snp	C/T			intron-variant	?	TAIR10	2:16890649	TGGGCTAGTCTGAGC[C/T]CATTGGGCTTGGGAT	818638
rs346728629	snp	C/T			synonymous-codon	?	TAIR10	2:16889530	ATCGACTCCAACTTT[C/T]TCTTTCCAGTATTTC	818638
rs346750262	snp	A/G			intron-variant	?	TAIR10	2:16890541	GTTCGAATCCCCACG[A/G]CTGCAAACACCTTAA	818638
rs346756309	snp	C/T			intron-variant	?	TAIR10	2:16890465	AATCATGAAACCACT[C/T]ATAGGTGGGCCAGTG	818638
rs346761912	snp	A/C/G/T			intron-variant	?	TAIR10	2:16890586	CAATTTAAAATCGGG[A/C/G/T]TATGCGGCCTCCAGG	818638
rs346762909	snp	A/G			intron-variant	?	TAIR10	2:16890682	CTGGGTTATCCAAAA[A/G]AAAAAAAAAAAAAAA	818638
rs346839879	snp	A/G			intron-variant	?	TAIR10	2:16889853	TCATTACTCCAAACA[A/G]TTAGCAATTTAGCAA	818638
rs346843289	snp	A/G			intron-variant	?	TAIR10	2:16890256	TTCGCATTAAGCGAA[A/G]TCTTGGAACCCTGGG	818638
rs346845240	snp	A/G			intron-variant	?	TAIR10	2:16890623	TCTTGCCGCTTTCGG[A/G]ACGCACGCAGTGGGC	818638
rs346855776	snp	A/C/G			intron-variant	?	TAIR10	2:16889805	ATCTAATTACTCATA[A/C/G]GTCTAATTGTGCATT	818638
rs346869561	snp	C/T			intron-variant	?	TAIR10	2:16890274	TTGGAACCCTGGGAA[C/T]CTCGGTGCTTAGCAC	818638
rs346920964	snp	C/T			intron-variant	?	TAIR10	2:16890331	GATTCTAGCACTCGT[C/T]GTACAAGTTAAAGCC	818638
rs346944094	snp	C/T			intron-variant	?	TAIR10	2:16890299	TAGCACTGACAACAG[C/T]GACCACATCTACTAC	818638
rs346978319	snp	A/G			intron-variant	?	TAIR10	2:16890270	AGTCTTGGAACCCTG[A/G]GAACCTCGGTGCTTA	818638
rs347018387	snp	C/G			intron-variant	?	TAIR10	2:16890420	AAGTAGAAATCGCAC[C/G]TAAATTAGTTATGAT	818638
rs347029342	snp	A/G			intron-variant	?	TAIR10	2:16890694	AAAAAAAAAAAAAAA[A/G]AAAAAAAGAAAGCGG	818638
rs347070549	snp	A/G			intron-variant	?	TAIR10	2:16890686	GTTATCCAAAAAAAA[A/G]AAAAAAAAAAAAAAA	818638
rs347093253	snp	A/G			missense	?	TAIR10	2:16891000	TCGTCTGACTCCAAC[A/G]TCTTCTTAAACACCT	818638
rs347221356	snp	A/T			intron-variant	?	TAIR10	2:16890035	TAATAATAATAAAAA[A/T]AAAAAAAATCTCTAA	818638
rs347261005	snp	C/T			intron-variant	?	TAIR10	2:16889365	CGATGATGCAGCCTT[C/T]GTAAAACACAATCCA	818638
rs347271860	snp	A/G			intron-variant	?	TAIR10	2:16890194	CATTTATTTAATTAC[A/G]GAATTATTTTATTTA	818638
rs347276530	snp	A/C/G			intron-variant	?	TAIR10	2:16890351	AAGTTAAAGCCTTCA[A/C/G]TATCTCCACTGTAAG	818638
rs347417175	snp	C/T			intron-variant	?	TAIR10	2:16889926	AATAGAAAAGTATTT[C/T]CCTGCTTCATCGCTT	818638
rs347440170	snp	A/T			intron-variant	?	TAIR10	2:16890090	AACTCCAGTAAAAAA[A/T]CATAAGATTATGAGA	818638