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rs121908388

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908388(C;T)
Make rs121908388(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position50792627
GeneCYLD
is asnp
is mentioned by
dbSNPrs121908388
ebirs121908388
HLIrs121908388
Exacrs121908388
Varsomers121908388
Maprs121908388
PheGenIrs121908388
hapmaprs121908388
1000 genomesrs121908388
hgdprs121908388
ensemblrs121908388
gopubmedrs121908388
geneviewrs121908388
scholarrs121908388
googlers121908388
pharmgkbrs121908388
gwascentralrs121908388
openSNPrs121908388
23andMers121908388
23andMe allrs121908388
SNP Nexus

SNPshotrs121908388
SNPdbers121908388
MSV3drs121908388
GWAS Ctlgrs121908388
Max Magnitude0
OMIM605018
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908388(T;T)
Alt rs121908388(T;T)
Reference rs121908388(C;C)
Significance Pathogenic
Disease Cylindromatosis not specified
Variation info
Gene CYLD
CLNDBN Cylindromatosis, familial not specified
Reversed 0
HGVS NC_000016.9:g.50826538C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005565.2, RCV000120624.1,