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: rs9895661
rs9895661
10 0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 0.700 1.000 5 2010 2018
dbSNP: rs11655024
rs11655024
2 17 61155004 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11657044
rs11657044
2 17 61372744 intron variant T/C snv 0.69 0.700 1.000 1 2016 2016