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: rs11691351
rs11691351
1 2 203009189 intron variant A/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs17406900
rs17406900
1 2 202919479 intron variant A/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs3731695
rs3731695
1 2 202955552 intron variant T/C snv 0.46 0.700 1.000 1 2011 2011
dbSNP: rs3845802
rs3845802
1 2 202875949 3 prime UTR variant T/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs3933629
rs3933629
1 2 202901644 intron variant T/C snv 0.39 0.700 1.000 1 2011 2011