Have questions? Visit https://www.reddit.com/r/SNPedia

rs886040887

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TAAAC;TAAAC) 0 common in clinvar
Make rs886040887(-;-)
Make rs886040887(-;AACTA)
Make rs886040887(AACTA;AACTA)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50792646
GeneCYLD, LOC105371251
is asnp
is mentioned by
dbSNPrs886040887
dbSNP (classic)rs886040887
ClinGenrs886040887
ebirs886040887
HLIrs886040887
Exacrs886040887
Gnomadrs886040887
Varsomers886040887
LitVarrs886040887
Maprs886040887
PheGenIrs886040887
Biobankrs886040887
1000 genomesrs886040887
hgdprs886040887
ensemblrs886040887
geneviewrs886040887
scholarrs886040887
googlers886040887
pharmgkbrs886040887
gwascentralrs886040887
openSNPrs886040887
23andMers886040887
SNPshotrs886040887
SNPdbers886040887
MSV3drs886040887
GWAS Ctlgrs886040887
Max Magnitude0
ClinVar
Risk rs886040887(-;-)
Alt rs886040887(-;-)
Reference Rs886040887(TAAAC;TAAAC)
Significance Pathogenic
Disease Cylindromatosis
Variation info
Gene CYLD
CLNDBN Cylindromatosis, familial
Reversed 0
HGVS NC_000016.9:g.50826557_50826561delAACTA
CLNSRC
CLNACC RCV000257950.1,