Product Details

SNP ID: rs17061686
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.6:132730151 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTTGAATAAAAAGGACAGATTAATG[A/G]CCTACTGGTTTAGACCTTTTCTTTT
Phenotype: MIM: 606592
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: VNN3 PubMed Links
Additional Information: For this assay, SNP(s) [rs540652229] 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_001291702.1		Intron			NP_001278631.1
NM_001291703.1		Intron			NP_001278632.1