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: rs7208487
rs7208487
4 0.925 0.080 17 39387196 intron variant T/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs8072297
rs8072297
1 17 39321795 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9916302
rs9916302
3 17 39343696 intron variant T/C snv 0.35 0.700 1.000 1 2016 2016