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: rs10892044
rs10892044
1 1.000 0.040 11 116896183 intron variant T/C snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11216186
rs11216186
1 1.000 0.040 11 116913976 intron variant T/C snv 7.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs11827828
rs11827828
1 1.000 0.040 11 116884868 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs12279433
rs12279433
1 1.000 0.040 11 116877505 intron variant G/T snv 7.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs2044426
rs2044426
1 1.000 0.040 11 116885467 intron variant G/A snv 7.1E-02 0.700 1.000 1 2018 2018