Product Details

SNP ID: rs13900
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.17:34256892 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: TTTCCCCTAGCTTTCCCCAGACACC[C/T]TGTTTTATTTTATTATAATGAATTT
Phenotype: MIM: 158105
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CCL2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002982.3	438	UTR 3			NP_002973.1