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: rs137853305
rs137853305
7 0.851 0.120 9 35685529 missense variant G/A snv 0.010 1.000 1 2007 2007
dbSNP: rs536639583
rs536639583
4 0.882 0.160 2 176092922 missense variant G/C snv 1.9E-04 6.7E-04 0.010 1.000 1 2018 2018
dbSNP: rs770627276
rs770627276
2 1.000 0.120 2 39120412 missense variant T/C snv 0.010 1.000 1 2018 2018