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: rs3130050
rs3130050
3 0.882 0.240 6 31650984 intron variant G/A snv 0.89 0.700 1.000 1 2010 2010
dbSNP: rs760293
rs760293
1 1.000 0.080 6 31644000 intron variant T/C snv 0.84 0.81 0.700 1.000 1 2007 2007