Product Details

SNP ID: rs8112989
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.19:2294280 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGTGAACACGGAGGCAGAGGCTAGG[G/T]TGACACAGCCACAAGCCGGGGATTG
Phenotype: MIM: 609792
Polymorphism: G/T, Transversion Substitution
Allele Nomenclature
Literature Links: LINGO3 PubMed Links
Additional Information: For this assay, SNP(s) [rs8113792] 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001101391.1		Intron			NP_001094861.1