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
5 0.790 0.280 17 37738049 intron variant A/G snv 0.52 0.870 1.000 3 2009 2019
dbSNP: rs11651052
rs11651052
2 0.851 0.200 17 37742390 intron variant G/A snv 0.50 0.800 1.000 1 2012 2019
dbSNP: rs11651755
rs11651755
2 0.763 0.160 17 37739849 intron variant T/C snv 0.52 0.800 1.000 1 2012 2018
dbSNP: rs11263763
rs11263763
2 0.882 0.200 17 37743574 intron variant A/G snv 0.43 0.700 1.000 1 2012 2012
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 2011 2011