rs267606736

Orientation

minus

Stabilized

minus

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

Make rs267606736(C;T)

Make rs267606736(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

100205167

Gene

CHUK

is a	snp
is	mentioned by
dbSNP	rs267606736
dbSNP (classic)	rs267606736
ClinGen	rs267606736
ebi	rs267606736
HLI	rs267606736
Exac	rs267606736
Gnomad	rs267606736
Varsome	rs267606736
LitVar	rs267606736
Map	rs267606736
PheGenI	rs267606736
Biobank	rs267606736
1000 genomes	rs267606736
hgdp	rs267606736
ensembl	rs267606736
geneview	rs267606736
scholar	rs267606736
google	rs267606736
pharmgkb	rs267606736
gwascentral	rs267606736
openSNP	rs267606736
23andMe	rs267606736
SNPshot	rs267606736
SNPdbe	rs267606736
MSV3d	rs267606736
GWAS Ctlg	rs267606736

Max Magnitude

0

ClinVar
Risk	rs267606736(T;T)
Alt	rs267606736(T;T)
Reference	Rs267606736(C;C)
Significance	Pathogenic
Disease	Cocoon syndrome
Variation	info
Gene	CHUK
CLNDBN	Cocoon syndrome
Reversed	1
HGVS	NC_000010.10:g.101964924G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009502.2,