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: rs879255368
rs879255368
5 19 41984953 missense variant C/G;T snv 0.700 0
dbSNP: rs387907281
rs387907281
13 0.752 0.280 19 41970284 missense variant C/T snv 0.700 0
dbSNP: rs80356537
rs80356537
17 0.752 0.320 19 41970405 missense variant C/A;G;T snv 0.700 0