rs886040890

Orientation

plus

Stabilized

plus

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

Make rs886040890(G;T)

Make rs886040890(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50792706

Gene	CYLD, LOC105371251

is a	snp
is	mentioned by
dbSNP	rs886040890
dbSNP (classic)	rs886040890
ClinGen	rs886040890
ebi	rs886040890
HLI	rs886040890
Exac	rs886040890
Gnomad	rs886040890
Varsome	rs886040890
LitVar	rs886040890
Map	rs886040890
PheGenI	rs886040890
Biobank	rs886040890
1000 genomes	rs886040890
hgdp	rs886040890
ensembl	rs886040890
geneview	rs886040890
scholar	rs886040890
google	rs886040890
pharmgkb	rs886040890
gwascentral	rs886040890
openSNP	rs886040890
23andMe	rs886040890
SNPshot	rs886040890
SNPdbe	rs886040890
MSV3d	rs886040890
GWAS Ctlg	rs886040890

Max Magnitude

0

ClinVar
Risk	rs886040890(T;T)
Alt	rs886040890(T;T)
Reference	Rs886040890(G;G)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50826617G>T
CLNSRC
CLNACC	RCV000257951.1,