rs121908388

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121908388(C;T)

Make rs121908388(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

50792627

Gene	CYLD, LOC105371251

is a	snp
is	mentioned by
dbSNP	rs121908388
dbSNP (classic)	rs121908388
ClinGen	rs121908388
ebi	rs121908388
HLI	rs121908388
Exac	rs121908388
Gnomad	rs121908388
Varsome	rs121908388
LitVar	rs121908388
Map	rs121908388
PheGenI	rs121908388
Biobank	rs121908388
1000 genomes	rs121908388
hgdp	rs121908388
ensembl	rs121908388
geneview	rs121908388
scholar	rs121908388
google	rs121908388
pharmgkb	rs121908388
gwascentral	rs121908388
openSNP	rs121908388
23andMe	rs121908388
SNPshot	rs121908388
SNPdbe	rs121908388
MSV3d	rs121908388
GWAS Ctlg	rs121908388

Max Magnitude

0

OMIM	605018
Desc
Variant	0002
Related	also

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,