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: rs104894502
rs104894502
6 0.807 0.120 15 63060915 missense variant A/G;T snv 0.010 1.000 1 2004 2004
dbSNP: rs199476306
rs199476306
3 0.882 0.080 15 63044100 missense variant C/T snv 0.010 1.000 1 2004 2004