Annotation Detail

Information
Associated Genes
CCL2 LOC126862536
Associated Variants
NC_000017.11:g.34252769A>G
NC_000017.11:g.34252769A>G
Associated Disease
Spina bifida, susceptibility to
Source Database
ClinVar
Description
NC_000017.11:g.34252769A>G AND Spina bifida, susceptibility to
ClinVar Allele ID
29246
Clinical Significance Description
risk factor
Clinical Significance Last Update
2009-01-15
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000015271
ClinVar Disease
Spina bifida, susceptibility to
Observed Origin Sample
germline
Pubmed
16596675
Pubmed
18940815
Pubmed
16352737
Pubmed
15466648
Pubmed
11500196
Drugs