Product Details
- SNP ID
-
rs884218
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:136953118 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- AGTGGCTCAGGTGCGCCATGGGCCC[T/C]GTCCCAGCACAGGCAGCTTCATGAC
- Phenotype
-
MIM: 120930
MIM: 609072
MIM: 612905
- Polymorphism
- T/C, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
C8G
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs115757662] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- C8G
- Gene Name
- complement component 8, gamma polypeptide
There are no transcripts associated with this gene.
- Gene
- FBXW5
- Gene Name
- F-box and WD repeat domain containing 5
There are no transcripts associated with this gene.
- Gene
- LCN12
- Gene Name
- lipocalin 12
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