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: rs9461856
rs9461856
2 1.000 0.040 6 33427422 intron variant G/A;T snv 0.700 1.000 3 2015 2019
dbSNP: rs875989808
rs875989808
3 0.925 0.160 6 33444529 missense variant C/T snv 0.700 0