Product Details

SNP ID

rs34593533

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:23947461 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATCATCCTTGTTGCCGTTTGGGAT[A/G]GAGCACCCAGAAGTGAACAGGCTCT

Phenotype

MIM: 602304

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

NR1D2 PubMed Links

Additional Information

For this assay, SNP(s) [rs201407165] 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

NR1D2

Gene Name

nuclear receptor subfamily 1 group D member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145425.1		Intron			NP_001138897.1
NM_005126.4		Intron			NP_005117.3
XM_006713451.3		Intron			XP_006713514.1

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