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rs886040893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs886040893(-;-)
Make rs886040893(-;T)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50794257
GeneCYLD, LOC105371251
is asnp
is mentioned by
dbSNPrs886040893
dbSNP (classic)rs886040893
ClinGenrs886040893
ebirs886040893
HLIrs886040893
Exacrs886040893
Gnomadrs886040893
Varsomers886040893
LitVarrs886040893
Maprs886040893
PheGenIrs886040893
Biobankrs886040893
1000 genomesrs886040893
hgdprs886040893
ensemblrs886040893
geneviewrs886040893
scholarrs886040893
googlers886040893
pharmgkbrs886040893
gwascentralrs886040893
openSNPrs886040893
23andMers886040893
SNPshotrs886040893
SNPdbers886040893
MSV3drs886040893
GWAS Ctlgrs886040893
Max Magnitude0
ClinVar
Risk rs886040893(-;-)
Alt rs886040893(-;-)
Reference Rs886040893(T;T)
Significance Pathogenic
Disease Cylindromatosis
Variation info
Gene CYLD
CLNDBN Cylindromatosis, familial
Reversed 0
HGVS NC_000016.9:g.50828168delT
CLNSRC
CLNACC RCV000257968.1,