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: rs4941246
rs4941246
1 1.000 0.040 18 64135070 intron variant C/T snv 0.60 0.700 1.000 1 2013 2013