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: rs7900522
rs7900522
1 1.000 0.040 10 76350213 intron variant T/A;C snv 0.700 1.000 1 2013 2013