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: rs1046089
rs1046089
4 0.882 0.200 6 31635190 missense variant G/A snv 0.36 0.40 0.700 1.000 1 2013 2013
dbSNP: rs2242660
rs2242660
2 0.925 0.160 6 31629976 intron variant G/A snv 0.46 0.700 1.000 1 2013 2013