Product Details

SNP ID

rs6474415

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:42707795 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCCTTGGGAAAAGACAAGAGGACC[A/G]TGAGGGGCACACGGCTGGTGTTCAG

Phenotype

MIM: 118508

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CHRNB3 PubMed Links

Additional Information

For this assay, SNP(s) [rs62516744] 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

CHRNB3

Gene Name

cholinergic receptor nicotinic beta 3 subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000749.3		Intron			NP_000740.1
XM_011544390.1		Intron			XP_011542692.1

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