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: rs3829251
rs3829251
8 0.851 0.120 11 71483513 intron variant G/A snv 0.21 0.800 1.000 1 2010 2010
dbSNP: rs11234027
rs11234027
5 0.882 0.080 11 71523061 intron variant G/A snv 0.24 0.700 1.000 1 2010 2010
dbSNP: rs12785878
rs12785878
25 0.677 0.520 11 71456403 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12800438
rs12800438
5 1.000 0.080 11 71459957 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4423214
rs4423214
2 11 71462208 intron variant C/T snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs4944062
rs4944062
2 11 71476248 3 prime UTR variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7938885
rs7938885
2 11 71458997 non coding transcript exon variant T/C snv 0.59 0.700 1.000 1 2018 2018