rs4738824

Orientation

plus

Stabilized

plus

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

Make rs4738824(A;G)

Make rs4738824(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

60777762

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs4738824
dbSNP (classic)	rs4738824
ClinGen	rs4738824
ebi	rs4738824
HLI	rs4738824
Exac	rs4738824
Gnomad	rs4738824
Varsome	rs4738824
LitVar	rs4738824
Map	rs4738824
PheGenI	rs4738824
Biobank	rs4738824
1000 genomes	rs4738824
hgdp	rs4738824
ensembl	rs4738824
geneview	rs4738824
scholar	rs4738824
google	rs4738824
pharmgkb	rs4738824
gwascentral	rs4738824
openSNP	rs4738824
23andMe	rs4738824
SNPshot	rs4738824
SNPdbe	rs4738824
MSV3d	rs4738824
GWAS Ctlg	rs4738824

GMAF

0.1758

Max Magnitude

0

OMIM	608892
Desc	CHROMODOMAIN HELICASE DNA-BINDING PROTEIN 7; CHD7
Variant
Related	also

OMIM	608892
Desc
Variant	0009
Related	also

[PMID 17436250] CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis.

ClinVar
Risk	rs4738824(G;G)
Alt	rs4738824(G;G)
Reference	Rs4738824(A;A)
Significance	Other
Disease	Scoliosis
Variation	info
Gene	CHD7
CLNDBN	Scoliosis, idiopathic 3
Reversed	0
HGVS	NC_000008.10:g.61690321A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002108.6,