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rs886040890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886040890(G;T)
Make rs886040890(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50792706
GeneCYLD, LOC105371251
is asnp
is mentioned by
dbSNPrs886040890
dbSNP (classic)rs886040890
ClinGenrs886040890
ebirs886040890
HLIrs886040890
Exacrs886040890
Gnomadrs886040890
Varsomers886040890
LitVarrs886040890
Maprs886040890
PheGenIrs886040890
Biobankrs886040890
1000 genomesrs886040890
hgdprs886040890
ensemblrs886040890
geneviewrs886040890
scholarrs886040890
googlers886040890
pharmgkbrs886040890
gwascentralrs886040890
openSNPrs886040890
23andMers886040890
SNPshotrs886040890
SNPdbers886040890
MSV3drs886040890
GWAS Ctlgrs886040890
Max Magnitude0
ClinVar
Risk rs886040890(T;T)
Alt rs886040890(T;T)
Reference Rs886040890(G;G)
Significance Pathogenic
Disease Cylindromatosis
Variation info
Gene CYLD
CLNDBN Cylindromatosis, familial
Reversed 0
HGVS NC_000016.9:g.50826617G>T
CLNSRC
CLNACC RCV000257951.1,