Product Details
- SNP ID
-
rs8121969
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.20:49813169 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GATCGGTCCCTCGAGCTGGGAATCT[A/C]CTGCCCAGCGCAGGCCCGGAGAGCT
- Phenotype
-
MIM: 612730
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
SLC9A8
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs77231829] 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
- SLC9A8
- Gene Name
- solute carrier family 9 member A8
View Full Product Details