Product Details

SNP ID: rs9512955
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.13:27987139 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CCATCTGGCTGTCAAAGGCCATCCT[A/G]ATAGGCGGCATCGTCTGTTGGCTCC
Phenotype: MIM: 615804
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: URAD PubMed Links
Additional Information: For this assay, SNP(s) [rs73453643] 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105577.1		Intron			NP_001099047.1