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rs4738824

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs4738824(A;G)
Make rs4738824(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position60777762
GeneCHD7
is asnp
is mentioned by
dbSNPrs4738824
ebirs4738824
HLIrs4738824
Exacrs4738824
Varsomers4738824
Maprs4738824
PheGenIrs4738824
hapmaprs4738824
1000 genomesrs4738824
hgdprs4738824
ensemblrs4738824
gopubmedrs4738824
geneviewrs4738824
scholarrs4738824
googlers4738824
pharmgkbrs4738824
gwascentralrs4738824
openSNPrs4738824
23andMers4738824
23andMe allrs4738824
SNP Nexus

SNPshotrs4738824
SNPdbers4738824
MSV3drs4738824
GWAS Ctlgrs4738824
GMAF0.1758
Max Magnitude0
OMIM608892
DescCHROMODOMAIN HELICASE DNA-BINDING PROTEIN 7; CHD7
Variant
Relatedalso
OMIM608892
Desc
Variant0009
Relatedalso
[PMID 17436250OA-icon.png] 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,