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: rs3087967
rs3087967
10 0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 0.710 1.000 3 2012 2019
dbSNP: rs11213809
rs11213809
1 1.000 0.080 11 111265020 intron variant A/G snv 0.74 0.700 1.000 1 2008 2008
dbSNP: rs7130173
rs7130173
1 1.000 0.080 11 111283347 intron variant A/C snv 0.70 0.010 1.000 1 2014 2014