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: rs11203495
rs11203495
1 8 13499310 missense variant T/G snv 0.85; 4.0E-06 0.85 0.010 1.000 1 2015 2015
dbSNP: rs1330010954
rs1330010954
4 0.882 0.080 8 13094897 missense variant C/T snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs372894000
rs372894000
4 0.882 0.080 8 13092766 missense variant C/T snv 2.0E-05 1.4E-05 0.010 1.000 1 2005 2005
dbSNP: rs3816747
rs3816747
2 1.000 0.080 8 13499293 missense variant G/A snv 0.87 0.89 0.010 1.000 1 2015 2015
dbSNP: rs756966085
rs756966085
4 0.882 0.080 8 13090431 missense variant C/T snv 8.0E-06 7.0E-06 0.010 1.000 1 2005 2005