Product Details

SNP ID

rs6965687

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:6332723 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCAAAAAATAAAAATTAAAATTAAA[A/G]AGCAGCAACACTGAAAGGATCAGCT

Phenotype

MIM: 616628

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM220A PubMed Links

Additional Information

For this assay, SNP(s) [rs76590486] 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

FAM220A

Gene Name

family with sequence similarity 220 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001037163.1		Intron			NP_001032240.1

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