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: rs59885338
rs59885338
4 0.851 0.120 1 156135268 missense variant C/T snv 3.6E-05 2.8E-05 0.700 1.000 5 2002 2008
dbSNP: rs11575937
rs11575937
14 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
dbSNP: rs59332535
rs59332535
5 0.827 0.160 1 156134911 missense variant G/A snv 0.700 0