Product Details

SNP ID
rs17131140
Assay Type
Functionally Tested
NCBI dbSNP Submissions
11
Location
Chr.1:90713638 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATGGGCATTTCCAACCGCACTTATG[A/G]ACGATTAGAACACAAACGGGAGAAA
Phenotype
MIM: 605212
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
BARHL2 PubMed Links
Additional Information
For this assay, SNP(s) [rs111253587] 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
BARHL2
Gene Name
BarH like homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020063.1 Intron NP_064447.1

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