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: rs1893217
rs1893217
14 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.850 1.000 9 2008 2016
dbSNP: rs514000
rs514000
1 1.000 0.040 18 12854073 intron variant C/T snv 0.71 0.710 1.000 1 2015 2015
dbSNP: rs12968719
rs12968719
6 0.827 0.120 18 12879467 intron variant G/A snv 8.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs62097857
rs62097857
5 0.827 0.120 18 12857759 intron variant G/A snv 2.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs657555
rs657555
4 0.925 0.080 18 12847137 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs80262450
rs80262450
2 1.000 0.040 18 12818923 intron variant G/A snv 8.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs7234029
rs7234029
7 0.807 0.320 18 12877061 intron variant A/G snv 0.27 0.020 1.000 2 2012 2014
dbSNP: rs200711300
rs200711300
3 0.925 0.040 18 12802118 missense variant A/C;G snv 1.6E-04; 4.0E-06 0.010 1.000 1 2012 2012