Source: BEFREE ×
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: rs28938168
rs28938168
2 1.000 0.160 11 117822424 missense variant C/T snv 0.020 1.000 2 2003 2015
dbSNP: rs121909262
rs121909262
5 0.851 0.120 3 122254304 missense variant C/G;T snv 0.010 1.000 1 1999 1999