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: rs11196172
rs11196172
18 0.708 0.200 10 112967084 intron variant G/A snv 0.13 0.700 1.000 4 2014 2019
dbSNP: rs11196170
rs11196170
10 0.776 0.080 10 112962862 intron variant G/A;C snv 0.700 1.000 1 2019 2019