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: rs104894345
rs104894345
6 0.827 0.080 12 119187080 missense variant G/C;T snv 0.020 1.000 2 2004 2006
dbSNP: rs104894351
rs104894351
7 0.827 0.080 12 119187078 missense variant A/C;G snv 0.020 1.000 2 2006 2011