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: rs121434587
rs121434587
1 1.000 0.080 6 160069961 missense variant G/T snv 0.700 0
dbSNP: rs121434588
rs121434588
1 1.000 0.080 6 160070006 missense variant G/A snv 0.700 0