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rs886040869

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs886040869(-;C)
Make rs886040869(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50754422
GeneCYLD
is asnp
is mentioned by
dbSNPrs886040869
dbSNP (classic)rs886040869
ClinGenrs886040869
ebirs886040869
HLIrs886040869
Exacrs886040869
Gnomadrs886040869
Varsomers886040869
LitVarrs886040869
Maprs886040869
PheGenIrs886040869
Biobankrs886040869
1000 genomesrs886040869
hgdprs886040869
ensemblrs886040869
geneviewrs886040869
scholarrs886040869
googlers886040869
pharmgkbrs886040869
gwascentralrs886040869
openSNPrs886040869
23andMers886040869
SNPshotrs886040869
SNPdbers886040869
MSV3drs886040869
GWAS Ctlgrs886040869
Max Magnitude0
ClinVar
Risk rs886040869(C;C)
Alt rs886040869(C;C)
Reference Rs886040869(-;-)
Significance Pathogenic
Disease Cylindromatosis
Variation info
Gene CYLD
CLNDBN Cylindromatosis, familial
Reversed 0
HGVS NC_000016.9:g.50788333dupC
CLNSRC
CLNACC RCV000257981.1,