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: rs4430796
rs4430796
14 0.790 0.280 17 37738049 intron variant A/G snv 0.52 0.800 1.000 1 2010 2010
dbSNP: rs11263761
rs11263761
2 1.000 0.080 17 37737784 intron variant A/G snv 0.44 0.700 1.000 1 2017 2017
dbSNP: rs11651052
rs11651052
7 0.851 0.200 17 37742390 intron variant G/A snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs3744763
rs3744763
3 0.925 0.160 17 37730894 non coding transcript exon variant A/G snv 0.30 0.700 1.000 1 2010 2010
dbSNP: rs7501939
rs7501939
12 0.776 0.280 17 37741165 intron variant C/T snv 0.41 0.700 1.000 1 2010 2010