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: rs387907223
rs387907223
1 1.000 0.240 11 2884129 missense variant A/C snv 0.800 1.000 2 2012 2013
dbSNP: rs387907226
rs387907226
1 1.000 0.240 11 2884123 missense variant T/C snv 0.800 1.000 2 2012 2014
dbSNP: rs318240750
rs318240750
3 0.925 0.240 11 2884119 missense variant C/A;G snv 0.800 1.000 1 2012 2012
dbSNP: rs387907224
rs387907224
1 1.000 0.240 11 2884128 missense variant A/G snv 0.800 1.000 1 2012 2012
dbSNP: rs387907225
rs387907225
1 1.000 0.240 11 2884670 missense variant C/T snv 0.800 1.000 1 2012 2012
dbSNP: rs515726203
rs515726203
1 1.000 0.240 11 2884675 missense variant A/C snv 0.710 1.000 1 2013 2013
dbSNP: rs886037912
rs886037912
1 1.000 0.240 11 2884113 missense variant C/A snv 0.700 1.000 1 2014 2014