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: rs7403531
rs7403531
1 1.000 0.080 15 38530704 intron variant T/C;G snv 0.77 0.820 1.000 1 2013 2015
dbSNP: rs11073333
rs11073333
1 1.000 0.080 15 38528446 intron variant G/A snv 0.76 0.700 1.000 1 2019 2019