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: rs2430561
rs2430561
14 0.724 0.393 12 68158742 intron variant T/A snp 0.36; 3.2E-05; 3.2E-05; 3.2E-05 0.010 1.000 1 2008 2008
dbSNP: rs3775291
rs3775291
30 0.647 0.464 4 186082920 missense variant C/G,T snp 1.2E-04; 0.28 1.6E-04; 0.24 0.010 1.000 1 2010 2010