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: rs3768080
rs3768080
3 0.882 0.040 1 236016569 intron variant A/G;T snv 0.810 1.000 1 2011 2011
dbSNP: rs10754833
rs10754833
4 0.851 0.040 1 236021631 intron variant T/A;C snv 0.010 1.000 1 2011 2011