rs886040874

Orientation

plus

Stabilized

plus

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

Make rs886040874(-;T)

Make rs886040874(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50781264

Gene

CYLD

is a	snp
is	mentioned by
dbSNP	rs886040874
dbSNP (classic)	rs886040874
ClinGen	rs886040874
ebi	rs886040874
HLI	rs886040874
Exac	rs886040874
Gnomad	rs886040874
Varsome	rs886040874
LitVar	rs886040874
Map	rs886040874
PheGenI	rs886040874
Biobank	rs886040874
1000 genomes	rs886040874
hgdp	rs886040874
ensembl	rs886040874
geneview	rs886040874
scholar	rs886040874
google	rs886040874
pharmgkb	rs886040874
gwascentral	rs886040874
openSNP	rs886040874
23andMe	rs886040874
SNPshot	rs886040874
SNPdbe	rs886040874
MSV3d	rs886040874
GWAS Ctlg	rs886040874

Max Magnitude

0

ClinVar
Risk	rs886040874(T;T)
Alt	rs886040874(T;T)
Reference	Rs886040874(-;-)
Significance	Pathogenic
Disease	Spiegler-Brooke syndrome
Variation	info
Gene	CYLD
CLNDBN	Spiegler-Brooke syndrome
Reversed	0
HGVS	NC_000016.9:g.50815175dupT
CLNSRC
CLNACC	RCV000257987.1,