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 9 2016 2019
dbSNP: rs11657044
rs11657044
2 17 61372744 intron variant T/C snv 0.69 0.700 1.000 2 2016 2019
dbSNP: rs11655024
rs11655024
2 17 61155004 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs2079742
rs2079742
9 0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs8073120
rs8073120
1 17 60854024 intron variant T/A snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs8080123
rs8080123
2 17 61165553 intron variant T/G snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs9903801
rs9903801
1 17 60837900 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs9907229
rs9907229
1 17 60840038 intron variant T/A;C snv 0.700 1.000 1 2019 2019