rs886040868

Orientation

plus

Stabilized

plus

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

Make rs886040868(-;-)

Make rs886040868(-;TGGA)

Make rs886040868(TGGA;TGGA)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50754342

Gene

CYLD

is a	snp
is	mentioned by
dbSNP	rs886040868
dbSNP (classic)	rs886040868
ClinGen	rs886040868
ebi	rs886040868
HLI	rs886040868
Exac	rs886040868
Gnomad	rs886040868
Varsome	rs886040868
LitVar	rs886040868
Map	rs886040868
PheGenI	rs886040868
Biobank	rs886040868
1000 genomes	rs886040868
hgdp	rs886040868
ensembl	rs886040868
geneview	rs886040868
scholar	rs886040868
google	rs886040868
pharmgkb	rs886040868
gwascentral	rs886040868
openSNP	rs886040868
23andMe	rs886040868
SNPshot	rs886040868
SNPdbe	rs886040868
MSV3d	rs886040868
GWAS Ctlg	rs886040868

Max Magnitude

0

ClinVar
Risk	rs886040868(-;-)
Alt	rs886040868(-;-)
Reference	Rs886040868(GGAT;GGAT)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50788253_50788256delTGGA
CLNSRC
CLNACC	RCV000257953.1,