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: rs8887
rs8887
7 1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 0.800 1.000 2 2012 2016
dbSNP: rs11673616
rs11673616
1 19 4506903 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs4991027
rs4991027
1 19 4509047 intron variant C/T snv 9.3E-02 0.700 1.000 1 2012 2012