Product Details

SNP ID: rs686868
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.5:76819347 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CTGGGCAGACGGTGGGATCCGGGCA[A/G]GTGTGCGAAGGCTGTTCTGCTGCCG
Phenotype: MIM: 600933
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: F2RL1 PubMed Links
Additional Information: For this assay, SNP(s) [rs111871548,rs113107082] 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
XM_017009223.1		Intron			XP_016864712.1