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: rs7944584
rs7944584
3 1.000 0.080 11 47314769 intron variant A/T snv 0.19 0.800 1.000 3 2010 2015
dbSNP: rs11039182
rs11039182
1 11 47325172 intron variant T/C snv 0.19 0.800 1.000 1 2012 2019
dbSNP: rs10501320
rs10501320
5 0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 0.700 1.000 1 2019 2019