Source: ALL
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: rs407934
rs407934
CARMIL1
3 0.925 0.120 6 25504334 intron variant C/T snv 0.34 0.700 1.000 1 2013 2013