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: rs1005300
rs1005300
1 1.000 0.120 22 39151886 intron variant C/G snv 0.68 0.700 1.000 1 2017 2017