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: rs4132601
rs4132601
9 0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 0.100 1.000 10 2009 2019
dbSNP: rs11978267
rs11978267
9 0.763 0.240 7 50398606 intron variant A/G snv 0.25 0.040 0.750 4 2013 2019
dbSNP: rs10235796
rs10235796
3 0.882 0.120 7 50394939 intron variant T/C snv 0.82 0.010 1.000 1 2017 2017
dbSNP: rs11980379
rs11980379
3 0.882 0.120 7 50402283 3 prime UTR variant T/C snv 0.25 0.010 < 0.001 1 2016 2016
dbSNP: rs6964969
rs6964969
4 0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 0.010 1.000 1 2017 2017