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: rs12939549
rs12939549
1 17 80637924 intron variant A/G snv 0.42 0.700 1.000 3 2015 2019
dbSNP: rs12940622
rs12940622
2 17 80641771 intron variant G/A snv 0.45 0.700 1.000 3 2015 2017
dbSNP: rs11150745
rs11150745
1 17 80783826 intron variant A/G snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs9910745
rs9910745
1 17 80636743 intron variant C/T snv 0.42 0.700 1.000 1 2019 2019