Product Details

SNP ID

rs2593813

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:186614782 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACACCTGGACATCATAAAATGCGGA[A/G]CTTCTCCCAGGGGAGGGGATGCTGA

Phenotype

MIM: 138680

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

AHSG PubMed Links

Additional Information

For this assay, SNP(s) [rs74451717] 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

AHSG

Gene Name

alpha 2-HS glycoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001622.2		Intron			NP_001613.2
XM_017005840.1		Intron			XP_016861329.1

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