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: rs11913239
rs11913239
1 1.000 0.160 22 30613852 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012