rs886040884

Orientation

plus

Stabilized

plus

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

Make rs886040884(A;A)

Make rs886040884(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50787852

Gene	CYLD, LOC105371251

is a	snp
is	mentioned by
dbSNP	rs886040884
dbSNP (classic)	rs886040884
ClinGen	rs886040884
ebi	rs886040884
HLI	rs886040884
Exac	rs886040884
Gnomad	rs886040884
Varsome	rs886040884
LitVar	rs886040884
Map	rs886040884
PheGenI	rs886040884
Biobank	rs886040884
1000 genomes	rs886040884
hgdp	rs886040884
ensembl	rs886040884
geneview	rs886040884
scholar	rs886040884
google	rs886040884
pharmgkb	rs886040884
gwascentral	rs886040884
openSNP	rs886040884
23andMe	rs886040884
SNPshot	rs886040884
SNPdbe	rs886040884
MSV3d	rs886040884
GWAS Ctlg	rs886040884

Max Magnitude

0

ClinVar
Risk	rs886040884(A;A)
Alt	rs886040884(A;A)
Reference	Rs886040884(G;G)
Significance	Pathogenic
Disease	Spiegler-Brooke syndrome
Variation	info
Gene	CYLD
CLNDBN	Spiegler-Brooke syndrome
Reversed	0
HGVS	NC_000016.9:g.50821763G>A
CLNSRC
CLNACC	RCV000257955.1,