Product Details
- SNP ID
-
rs990192
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:86574165 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GCTTGGGGGGGAAAATAACTGCCAG[T/G]CGAAAAGCATAAATTGCAATGGTCT
- Phenotype
-
MIM: 605080
- Polymorphism
- T/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
CNGB3
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs28471019] are located under a probe 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
- CNGB3
- Gene Name
- cyclic nucleotide gated channel beta 3
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