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: rs920778
rs920778
36 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.040 1.000 4 2015 2017
dbSNP: rs12427129
rs12427129
2 1.000 0.080 12 53973906 missense variant C/T snv 9.0E-02 7.0E-02 0.010 1.000 1 2019 2019
dbSNP: rs4759314
rs4759314
31 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 0.010 1.000 1 2019 2019