rs886040885

Orientation

plus

Stabilized

plus

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

Make rs886040885(-;AC)

Make rs886040885(AC;AC)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50791588

Gene	CYLD, LOC105371251

is a	snp
is	mentioned by
dbSNP	rs886040885
dbSNP (classic)	rs886040885
ClinGen	rs886040885
ebi	rs886040885
HLI	rs886040885
Exac	rs886040885
Gnomad	rs886040885
Varsome	rs886040885
LitVar	rs886040885
Map	rs886040885
PheGenI	rs886040885
Biobank	rs886040885
1000 genomes	rs886040885
hgdp	rs886040885
ensembl	rs886040885
geneview	rs886040885
scholar	rs886040885
google	rs886040885
pharmgkb	rs886040885
gwascentral	rs886040885
openSNP	rs886040885
23andMe	rs886040885
SNPshot	rs886040885
SNPdbe	rs886040885
MSV3d	rs886040885
GWAS Ctlg	rs886040885

Max Magnitude

0

ClinVar
Risk	rs886040885(AC;AC)
Alt	rs886040885(AC;AC)
Reference	Rs886040885(-;-)
Significance	Pathogenic
Disease	Spiegler-Brooke syndrome
Variation	info
Gene	CYLD
CLNDBN	Spiegler-Brooke syndrome
Reversed	0
HGVS	NC_000016.9:g.50825498_50825499dupAC
CLNSRC
CLNACC	RCV000257982.1,