rs886040894

Orientation

plus

Stabilized

plus

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

Make rs886040894(C;T)

Make rs886040894(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50794311

Gene	CYLD, LOC105371251

is a	snp
is	mentioned by
dbSNP	rs886040894
dbSNP (classic)	rs886040894
ClinGen	rs886040894
ebi	rs886040894
HLI	rs886040894
Exac	rs886040894
Gnomad	rs886040894
Varsome	rs886040894
LitVar	rs886040894
Map	rs886040894
PheGenI	rs886040894
Biobank	rs886040894
1000 genomes	rs886040894
hgdp	rs886040894
ensembl	rs886040894
geneview	rs886040894
scholar	rs886040894
google	rs886040894
pharmgkb	rs886040894
gwascentral	rs886040894
openSNP	rs886040894
23andMe	rs886040894
SNPshot	rs886040894
SNPdbe	rs886040894
MSV3d	rs886040894
GWAS Ctlg	rs886040894

Max Magnitude

0

ClinVar
Risk	rs886040894(T;T)
Alt	rs886040894(T;T)
Reference	Rs886040894(C;C)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50828222C>T
CLNSRC
CLNACC	RCV000257992.1,