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: rs2302264
rs2302264
1 11 67439955 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs869736
rs869736
3 0.925 0.080 11 67437991 3 prime UTR variant C/A snv 0.53 0.700 1.000 1 2012 2012