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rs886040892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs886040892(-;-)
Make rs886040892(-;CT)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50793601
GeneCYLD, LOC105371251
is asnp
is mentioned by
dbSNPrs886040892
dbSNP (classic)rs886040892
ClinGenrs886040892
ebirs886040892
HLIrs886040892
Exacrs886040892
Gnomadrs886040892
Varsomers886040892
LitVarrs886040892
Maprs886040892
PheGenIrs886040892
Biobankrs886040892
1000 genomesrs886040892
hgdprs886040892
ensemblrs886040892
geneviewrs886040892
scholarrs886040892
googlers886040892
pharmgkbrs886040892
gwascentralrs886040892
openSNPrs886040892
23andMers886040892
SNPshotrs886040892
SNPdbers886040892
MSV3drs886040892
GWAS Ctlgrs886040892
Max Magnitude0
ClinVar
Risk rs886040892(-;-)
Alt rs886040892(-;-)
Reference Rs886040892(CT;CT)
Significance Pathogenic
Disease Cylindromatosis
Variation info
Gene CYLD
CLNDBN Cylindromatosis, familial
Reversed 0
HGVS NC_000016.9:g.50827512_50827513delCT
CLNSRC
CLNACC RCV000257939.1,