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: rs10832169
rs10832169
1 11 14044939 intron variant G/A snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs11023056
rs11023056
1 11 14030572 intron variant A/G snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs2618521
rs2618521
1 11 14031785 intron variant A/G snv 0.66 0.700 1.000 1 2018 2018