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: rs169068
rs169068
12 0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 0.010 1.000 1 2011 2011
dbSNP: rs34037914
rs34037914
1 1.000 0.120 16 1079501 synonymous variant C/T snv 5.9E-02 4.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs642249
rs642249
1 1.000 0.120 16 1079912 synonymous variant A/G snv 0.96 0.96 0.010 1.000 1 2011 2011