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rs886040891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs886040891(-;-)
Make rs886040891(-;AT)
Make rs886040891(AT;AT)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50793585
GeneCYLD, LOC105371251
is asnp
is mentioned by
dbSNPrs886040891
dbSNP (classic)rs886040891
ClinGenrs886040891
ebirs886040891
HLIrs886040891
Exacrs886040891
Gnomadrs886040891
Varsomers886040891
LitVarrs886040891
Maprs886040891
PheGenIrs886040891
Biobankrs886040891
1000 genomesrs886040891
hgdprs886040891
ensemblrs886040891
geneviewrs886040891
scholarrs886040891
googlers886040891
pharmgkbrs886040891
gwascentralrs886040891
openSNPrs886040891
23andMers886040891
SNPshotrs886040891
SNPdbers886040891
MSV3drs886040891
GWAS Ctlgrs886040891
Max Magnitude0
ClinVar
Risk rs886040891(-;-)
Alt rs886040891(-;-)
Reference Rs886040891(TA;TA)
Significance Pathogenic
Disease Cylindromatosis
Variation info
Gene CYLD
CLNDBN Cylindromatosis, familial
Reversed 0
HGVS NC_000016.9:g.50827496_50827497delAT
CLNSRC
CLNACC RCV000257985.1,