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: rs12149527
rs12149527
1 1.000 0.080 16 79076699 intron variant C/T snv 0.36 0.700 1.000 1 2013 2013