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: rs11216230
rs11216230
2 11 117014073 intron variant G/A snv 3.1E-02 0.800 1.000 3 2014 2019
dbSNP: rs12225230
rs12225230
4 11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06 0.800 1.000 2 2012 2018
dbSNP: rs11216162
rs11216162
3 11 116857561 non coding transcript exon variant G/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs139961185
rs139961185
2 11 116936627 intron variant G/A snv 1.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs7115242
rs7115242
16 0.851 0.120 11 117037567 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7115583
rs7115583
1 11 116913660 intron variant G/T snv 0.17 0.700 1.000 1 2019 2019