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: rs9303277
rs9303277
3 0.790 0.240 17 39820216 intron variant C/T snv 0.52 0.800 1.000 4 2010 2017
dbSNP: rs4795395
rs4795395
1 1.000 0.080 17 39806734 intron variant T/A snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs9635726
rs9635726
1 0.925 0.160 17 39863888 intron variant C/T snv 0.18 0.700 1.000 1 2017 2017