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rs886040888

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs886040888(A;T)
Make rs886040888(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50792654
GeneCYLD, LOC105371251
is asnp
is mentioned by
dbSNPrs886040888
dbSNP (classic)rs886040888
ClinGenrs886040888
ebirs886040888
HLIrs886040888
Exacrs886040888
Gnomadrs886040888
Varsomers886040888
LitVarrs886040888
Maprs886040888
PheGenIrs886040888
Biobankrs886040888
1000 genomesrs886040888
hgdprs886040888
ensemblrs886040888
geneviewrs886040888
scholarrs886040888
googlers886040888
pharmgkbrs886040888
gwascentralrs886040888
openSNPrs886040888
23andMers886040888
SNPshotrs886040888
SNPdbers886040888
MSV3drs886040888
GWAS Ctlgrs886040888
Max Magnitude0
ClinVar
Risk rs886040888(T;T)
Alt rs886040888(T;T)
Reference Rs886040888(A;A)
Significance Pathogenic
Disease Cylindromatosis
Variation info
Gene CYLD
CLNDBN Cylindromatosis, familial
Reversed 0
HGVS NC_000016.9:g.50826565A>T
CLNSRC
CLNACC RCV000257977.1,