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: rs11601507
rs11601507
3 1.000 0.040 11 5679844 missense variant C/A;T snv 9.3E-02; 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs12271225
rs12271225
1 11 5669314 intron variant A/G;T snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs3824949
rs3824949
1 11 5680179 5 prime UTR variant G/C snv 0.51 0.43 0.700 1.000 1 2016 2016