Product Details
- SNP ID
-
rs413781
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:2904391 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- AGGGTGAGCCTAAGGATCCCTCCCC[G/T]CCGTGCCTCAGGCGCCCCGCCCACT
- Phenotype
-
MIM: 602631
MIM: 603240
- Polymorphism
- G/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
SLC22A18
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs80093400] 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
- SLC22A18
- Gene Name
- solute carrier family 22 member 18
- Gene
- SLC22A18AS
- Gene Name
- solute carrier family 22 member 18 antisense
View Full Product Details