rs764952788

Orientation

plus

Stabilized

plus

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

Make rs764952788(A;A)

Make rs764952788(A;C)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50779853

Gene

CYLD

is a	snp
is	mentioned by
dbSNP	rs764952788
dbSNP (classic)	rs764952788
ClinGen	rs764952788
ebi	rs764952788
HLI	rs764952788
Exac	rs764952788
Gnomad	rs764952788
Varsome	rs764952788
LitVar	rs764952788
Map	rs764952788
PheGenI	rs764952788
Biobank	rs764952788
1000 genomes	rs764952788
hgdp	rs764952788
ensembl	rs764952788
geneview	rs764952788
scholar	rs764952788
google	rs764952788
pharmgkb	rs764952788
gwascentral	rs764952788
openSNP	rs764952788
23andMe	rs764952788
SNPshot	rs764952788
SNPdbe	rs764952788
MSV3d	rs764952788
GWAS Ctlg	rs764952788

Max Magnitude

0

ClinVar
Risk	rs764952788(A;A) rs764952788(T;T)
Alt	rs764952788(A;A) rs764952788(T;T)
Reference	Rs764952788(C;C)
Significance	Pathogenic
Disease	Cylindromatosis
Variation	info
Gene	CYLD
CLNDBN	Cylindromatosis, familial
Reversed	0
HGVS	NC_000016.9:g.50813764C>T
CLNSRC
CLNACC	RCV000257934.1,