rs886040886

Orientation

plus

Stabilized

plus

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

Make rs886040886(A;G)

Make rs886040886(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50792595

Gene	CYLD, LOC105371251

is a	snp
is	mentioned by
dbSNP	rs886040886
dbSNP (classic)	rs886040886
ClinGen	rs886040886
ebi	rs886040886
HLI	rs886040886
Exac	rs886040886
Gnomad	rs886040886
Varsome	rs886040886
LitVar	rs886040886
Map	rs886040886
PheGenI	rs886040886
Biobank	rs886040886
1000 genomes	rs886040886
hgdp	rs886040886
ensembl	rs886040886
geneview	rs886040886
scholar	rs886040886
google	rs886040886
pharmgkb	rs886040886
gwascentral	rs886040886
openSNP	rs886040886
23andMe	rs886040886
SNPshot	rs886040886
SNPdbe	rs886040886
MSV3d	rs886040886
GWAS Ctlg	rs886040886

Max Magnitude

0

ClinVar
Risk	rs886040886(G;G)
Alt	rs886040886(G;G)
Reference	Rs886040886(A;A)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50826506A>G
CLNSRC
CLNACC	RCV000258001.1,