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: rs838880
rs838880
3 12 124777047 3 prime UTR variant C/T snv 0.55 0.700 1.000 2 2010 2013
dbSNP: rs10773105
rs10773105
2 12 124799220 intron variant C/T snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs10773112
rs10773112
2 12 124853983 intron variant C/T snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs10846743
rs10846743
2 12 124825759 intron variant G/A snv 3.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs12580323
rs12580323
2 12 124795115 intron variant C/T snv 1.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs12819677
rs12819677
2 12 124798975 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7137923
rs7137923
2 12 124822302 intron variant G/T snv 3.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs865716
rs865716
2 12 124806310 intron variant A/T snv 0.58 0.700 1.000 1 2012 2012