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: rs10744777
rs10744777
1 1.000 0.080 12 111795214 intron variant T/C snv 0.53 0.720 1.000 3 2014 2018