Product Details

SNP ID
rs6866492
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:40916026 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGAGTTATAAATTGGATGCATTTG[A/G]TATTCTTAGAGAATCAGTAAAGATT
Phenotype
MIM: 217070
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C7 PubMed Links

Gene Details

Gene
C7
Gene Name
complement component 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000587.2 Intron NP_000578.2

View Full Product Details