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: rs76097649
rs76097649
1 1.000 0.080 11 128894675 intron variant G/A snv 7.9E-02 0.700 1.000 2 2018 2018
dbSNP: rs75190942
rs75190942
2 1.000 0.080 11 128894676 intron variant C/A snv 7.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs6590357
rs6590357
3 0.882 0.120 11 128911444 synonymous variant T/C snv 0.84 0.85 0.010 1.000 1 2017 2017