rs886040879

Orientation

plus

Stabilized

plus

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

Make rs886040879(A;T)

Make rs886040879(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50782411

Gene

CYLD

is a	snp
is	mentioned by
dbSNP	rs886040879
dbSNP (classic)	rs886040879
ClinGen	rs886040879
ebi	rs886040879
HLI	rs886040879
Exac	rs886040879
Gnomad	rs886040879
Varsome	rs886040879
LitVar	rs886040879
Map	rs886040879
PheGenI	rs886040879
Biobank	rs886040879
1000 genomes	rs886040879
hgdp	rs886040879
ensembl	rs886040879
geneview	rs886040879
scholar	rs886040879
google	rs886040879
pharmgkb	rs886040879
gwascentral	rs886040879
openSNP	rs886040879
23andMe	rs886040879
SNPshot	rs886040879
SNPdbe	rs886040879
MSV3d	rs886040879
GWAS Ctlg	rs886040879

Max Magnitude

0

ClinVar
Risk	rs886040879(T;T)
Alt	rs886040879(T;T)
Reference	Rs886040879(A;A)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50816322A>T
CLNSRC
CLNACC	RCV000257974.1,