rs886040892

Orientation

plus

Stabilized

plus

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

Make rs886040892(-;-)

Make rs886040892(-;CT)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50793601

Gene	CYLD, LOC105371251

is a	snp
is	mentioned by
dbSNP	rs886040892
dbSNP (classic)	rs886040892
ClinGen	rs886040892
ebi	rs886040892
HLI	rs886040892
Exac	rs886040892
Gnomad	rs886040892
Varsome	rs886040892
LitVar	rs886040892
Map	rs886040892
PheGenI	rs886040892
Biobank	rs886040892
1000 genomes	rs886040892
hgdp	rs886040892
ensembl	rs886040892
geneview	rs886040892
scholar	rs886040892
google	rs886040892
pharmgkb	rs886040892
gwascentral	rs886040892
openSNP	rs886040892
23andMe	rs886040892
SNPshot	rs886040892
SNPdbe	rs886040892
MSV3d	rs886040892
GWAS Ctlg	rs886040892

Max Magnitude

0

ClinVar
Risk	rs886040892(-;-)
Alt	rs886040892(-;-)
Reference	Rs886040892(CT;CT)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50827512_50827513delCT
CLNSRC
CLNACC	RCV000257939.1,