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: rs3825932
rs3825932
6 0.827 0.360 15 78943104 intron variant T/C snv 0.50 0.800 1.000 2 2008 2009
dbSNP: rs34593439
rs34593439
2 1.000 0.120 15 78942615 intron variant G/A;C snv 0.10 0.700 1.000 1 2015 2015