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: rs58922911
rs58922911
2 0.925 0.320 1 156115094 missense variant T/G snv 0.800 1.000 3 2003 2009
dbSNP: rs28928903
rs28928903
2 0.925 0.240 1 156115087 missense variant G/A;C snv 0.800 0
dbSNP: rs11575937
rs11575937
29 0.653 0.480 1 156136985 missense variant G/A;T snv 0.700 0
dbSNP: rs386134243
rs386134243
16 0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 0.700 0