rs886040876

Orientation

plus

Stabilized

plus

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

Make rs886040876(-;-)

Make rs886040876(-;ATCA)

Make rs886040876(ATCA;ATCA)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50781385

Gene

CYLD

is a	snp
is	mentioned by
dbSNP	rs886040876
dbSNP (classic)	rs886040876
ClinGen	rs886040876
ebi	rs886040876
HLI	rs886040876
Exac	rs886040876
Gnomad	rs886040876
Varsome	rs886040876
LitVar	rs886040876
Map	rs886040876
PheGenI	rs886040876
Biobank	rs886040876
1000 genomes	rs886040876
hgdp	rs886040876
ensembl	rs886040876
geneview	rs886040876
scholar	rs886040876
google	rs886040876
pharmgkb	rs886040876
gwascentral	rs886040876
openSNP	rs886040876
23andMe	rs886040876
SNPshot	rs886040876
SNPdbe	rs886040876
MSV3d	rs886040876
GWAS Ctlg	rs886040876

Max Magnitude

0

ClinVar
Risk	rs886040876(-;-)
Alt	rs886040876(-;-)
Reference	Rs886040876(CAAT;CAAT)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50815296_50815299delATCA
CLNSRC
CLNACC	RCV000257967.1,