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: rs35829419
rs35829419
23 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 0.030 0.667 3 2009 2016
dbSNP: rs10754558
rs10754558
20 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 0.020 1.000 2 2014 2018
dbSNP: rs10925019
rs10925019
2 0.925 0.040 1 247432548 intron variant C/T snv 0.11 0.020 1.000 2 2010 2014
dbSNP: rs4925648
rs4925648
2 0.925 0.040 1 247417266 intron variant C/T snv 0.12 0.010 1.000 1 2010 2010