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: rs1800469
rs1800469
78 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.810 1.000 4 2014 2018
dbSNP: rs2241716
rs2241716
2 1.000 0.080 19 41348181 intron variant C/T snv 4.0E-02 0.700 1.000 1 2014 2014
dbSNP: rs767685429
rs767685429
3 0.882 0.120 19 41332206 missense variant G/A;C snv 2.8E-05; 8.0E-06 0.010 < 0.001 1 2009 2009