rs886040872

Orientation

plus

Stabilized

plus

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

Make rs886040872(A;A)

Make rs886040872(A;C)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50777915

Gene

CYLD

is a	snp
is	mentioned by
dbSNP	rs886040872
dbSNP (classic)	rs886040872
ClinGen	rs886040872
ebi	rs886040872
HLI	rs886040872
Exac	rs886040872
Gnomad	rs886040872
Varsome	rs886040872
LitVar	rs886040872
Map	rs886040872
PheGenI	rs886040872
Biobank	rs886040872
1000 genomes	rs886040872
hgdp	rs886040872
ensembl	rs886040872
geneview	rs886040872
scholar	rs886040872
google	rs886040872
pharmgkb	rs886040872
gwascentral	rs886040872
openSNP	rs886040872
23andMe	rs886040872
SNPshot	rs886040872
SNPdbe	rs886040872
MSV3d	rs886040872
GWAS Ctlg	rs886040872

Max Magnitude

0

ClinVar
Risk	rs886040872(A;A)
Alt	rs886040872(A;A)
Reference	Rs886040872(C;C)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50811826C>A
CLNSRC
CLNACC	RCV000257976.1,