Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3771341
rs3771341
3 2 233764593 intron variant G/A;T snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs4663333
rs4663333
3 2 233746657 intron variant G/T snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs6742078
rs6742078
13 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs7564935
rs7564935
3 2 233736540 intron variant G/T snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs10178992
rs10178992
4 2 233749231 intron variant T/A snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs4124874
rs4124874
8 0.851 0.120 2 233757013 intron variant T/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs4148324
rs4148324
4 2 233764076 intron variant T/A;G snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs10179091
rs10179091
4 2 233749337 intron variant T/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs11888459
rs11888459
4 2 233747994 non coding transcript exon variant T/C snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs1983023
rs1983023
3 2 233728376 intron variant T/C snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs3806596
rs3806596
3 2 233729061 intron variant T/C snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs4148326
rs4148326
5 0.925 0.080 2 233764816 intron variant T/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs4663965
rs4663965
3 2 233741958 intron variant T/C snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs6714634
rs6714634
4 2 233756119 non coding transcript exon variant T/C snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs6715325
rs6715325
3 2 233726595 intron variant T/C snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs871514
rs871514
3 2 233719883 intron variant T/C snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs4399719
rs4399719
3 2 233757815 intron variant T/G snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs4663963
rs4663963
3 2 233741547 non coding transcript exon variant T/G snv 0.55 0.700 1.000 1 2013 2013