Product Details

SNP ID: rs12462820
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.19:47826288 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGTGATCCCGGGTAAGTCACACTTT[C/T]GAGCCTGAAGATGTTCTCTAAACTG
Phenotype: MIM: 602225
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: CRX PubMed Links
Additional Information: For this assay, SNP(s) [rs146640075] 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

There are no transcripts associated with this gene.