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: rs267606976
rs267606976
2 1.000 0.080 7 151564203 missense variant A/G snv 0.700 1.000 2 2005 2014
dbSNP: rs121908987
rs121908987
12 0.742 0.200 7 151576412 missense variant C/A;G;T snv 4.0E-06 0.700 0
dbSNP: rs193922697
rs193922697
2 1.000 0.040 7 151576438 missense variant G/A;T snv 1.6E-05 0.700 0
dbSNP: rs121908989
rs121908989
4 0.882 0.080 7 151564199 missense variant T/A;C snv 4.0E-06 0.010 1.000 1 2005 2005