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: rs1130866
rs1130866
9 0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 0.030 1.000 3 2000 2006
dbSNP: rs7316
rs7316
3 0.882 0.160 2 85658890 3 prime UTR variant T/C snv 0.14 0.010 1.000 1 2018 2018