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: rs121909250
rs121909250
1 1.000 0.040 13 110719736 missense variant G/C snv 0.700 0
dbSNP: rs121909251
rs121909251
1 1.000 0.040 13 110719739 missense variant A/G snv 0.700 0
dbSNP: rs121909252
rs121909252
1 1.000 0.040 13 110719667 missense variant C/A snv 0.700 0