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: rs10892354
rs10892354
1 11 119367671 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11217257
rs11217257
1 11 119367745 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs2195525
rs2195525
1 11 119364694 intron variant C/T snv 0.52 0.700 1.000 1 2019 2019