Product Details
- SNP ID
-
rs149843
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:38285166 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTTTTGGCTGTGGAAAATACTAAGA[A/G]CAAGTAGTAGCAGGCAGAAGTTCAC
- Phenotype
-
MIM: 604047
MIM: 604048
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
SLC22A13
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs111389039] 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
- SLC22A13
- Gene Name
- solute carrier family 22 member 13
There are no transcripts associated with this gene.
- Gene
- SLC22A14
- Gene Name
- solute carrier family 22 member 14
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