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: rs1918690
rs1918690
1 1.000 0.120 2 84679791 intron variant T/C snv 0.74 0.700 1.000 1 2014 2014