Product Details
- SNP ID
-
rs653286
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
41
- Location
-
Chr.1:22645091 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GCGGAGGTGATGGGGTGACAGAGGC[A/G]GTGGAAAGGAGGGAGGCCAGTTGAG
- Phenotype
-
MIM: 120550
MIM: 120570
MIM: 120575
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
C1QA
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs72877151] 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
- C1QA
- Gene Name
- complement C1q A chain
There are no transcripts associated with this gene.
- Gene
- C1QB
- Gene Name
- complement C1q B chain
There are no transcripts associated with this gene.
- Gene
- C1QC
- Gene Name
- complement C1q C chain
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