rs886040875

Orientation

plus

Stabilized

plus

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

Make rs886040875(-;T)

Make rs886040875(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50781326

Gene

CYLD

is a	snp
is	mentioned by
dbSNP	rs886040875
dbSNP (classic)	rs886040875
ClinGen	rs886040875
ebi	rs886040875
HLI	rs886040875
Exac	rs886040875
Gnomad	rs886040875
Varsome	rs886040875
LitVar	rs886040875
Map	rs886040875
PheGenI	rs886040875
Biobank	rs886040875
1000 genomes	rs886040875
hgdp	rs886040875
ensembl	rs886040875
geneview	rs886040875
scholar	rs886040875
google	rs886040875
pharmgkb	rs886040875
gwascentral	rs886040875
openSNP	rs886040875
23andMe	rs886040875
SNPshot	rs886040875
SNPdbe	rs886040875
MSV3d	rs886040875
GWAS Ctlg	rs886040875

Max Magnitude

0

ClinVar
Risk	rs886040875(T;T)
Alt	rs886040875(T;T)
Reference	Rs886040875(-;-)
Significance	Pathogenic
Disease	Spiegler-Brooke syndrome
Variation	info
Gene	CYLD
CLNDBN	Spiegler-Brooke syndrome
Reversed	0
HGVS	NC_000016.9:g.50815237dupT
CLNSRC
CLNACC	RCV000257947.1,