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: rs180177040
rs180177040
9 0.790 0.360 7 140754187 missense variant T/C;G snv 0.700 1.000 8 1968 2013
dbSNP: rs180177041
rs180177041
5 0.851 0.240 7 140777006 missense variant C/G snv 0.700 1.000 8 1968 2013
dbSNP: rs180177042
rs180177042
8 0.807 0.280 7 140749365 missense variant A/C;T snv 0.700 1.000 8 1968 2013
dbSNP: rs397516893
rs397516893
3 0.925 0.160 7 140778048 missense variant A/C snv 0.700 1.000 8 1968 2013
dbSNP: rs869025340
rs869025340
5 0.925 0.160 7 140777032 missense variant A/C;G;T snv 0.700 1.000 8 1968 2013
dbSNP: rs121913348
rs121913348
20 0.763 0.480 7 140781617 missense variant C/A;G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs180177035
rs180177035
35 0.752 0.280 7 140801502 missense variant T/C snv 0.700 0