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: rs11048456
rs11048456
6 1.000 0.080 12 26310149 intron variant C/T snv 0.62 0.700 1.000 2 2018 2018