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: rs146776939
rs146776939
3 0.882 0.080 11 101504595 missense variant T/C snv 2.0E-04 2.2E-04 0.010 1.000 1 2011 2011
dbSNP: rs760415536
rs760415536
2 0.925 0.080 11 101583445 missense variant C/G snv 7.0E-06 0.010 1.000 1 2019 2019