rs886040873

Orientation

plus

Stabilized

plus

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

Make rs886040873(C;T)

Make rs886040873(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50779889

Gene

CYLD

is a	snp
is	mentioned by
dbSNP	rs886040873
dbSNP (classic)	rs886040873
ClinGen	rs886040873
ebi	rs886040873
HLI	rs886040873
Exac	rs886040873
Gnomad	rs886040873
Varsome	rs886040873
LitVar	rs886040873
Map	rs886040873
PheGenI	rs886040873
Biobank	rs886040873
1000 genomes	rs886040873
hgdp	rs886040873
ensembl	rs886040873
geneview	rs886040873
scholar	rs886040873
google	rs886040873
pharmgkb	rs886040873
gwascentral	rs886040873
openSNP	rs886040873
23andMe	rs886040873
SNPshot	rs886040873
SNPdbe	rs886040873
MSV3d	rs886040873
GWAS Ctlg	rs886040873

Max Magnitude

0

ClinVar
Risk	rs886040873(T;T)
Alt	rs886040873(T;T)
Reference	Rs886040873(C;C)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50813800C>T
CLNSRC
CLNACC	RCV000257960.1,