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: rs11708067
rs11708067
9 0.882 0.080 3 123346931 intron variant A/G snv 0.19 0.840 0.875 8 2010 2018
dbSNP: rs11720108
rs11720108
1 1.000 0.080 3 123350211 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11717195
rs11717195
3 1.000 0.080 3 123363551 intron variant T/C snv 0.19 0.800 1.000 2 2012 2014