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: rs12209887
rs12209887
1 6 100708930 intron variant G/A snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs180963
rs180963
1 6 100679337 intron variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs6907240
rs6907240
1 6 100705906 intron variant T/C;G snv 0.700 1.000 1 2019 2019