Product Details

SNP ID

rs7590874

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:76750644 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTCTTATGGCTCCCTATACTGCAGG[G/T]AGTTAACCAGTCTTAAATATAATTC

Phenotype

MIM: 610870

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

LRRTM4 PubMed Links

Additional Information

For this assay, SNP(s) [rs76543253,rs77073950] 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

LRRTM4

Gene Name

leucine rich repeat transmembrane neuronal 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011533117.2		Intron			XP_011531419.1

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