Product Details

SNP ID

rs16840394

Assay Type

Functionally Tested

NCBI dbSNP Submissions

12

Location

Chr.1:196659065 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAATGAGAAAAATGAGATGGCTAT[A/T]TCTTTTAGTTTTAAGATAAATCACA

Phenotype

MIM: 134370

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

CFH PubMed Links

Additional Information

For this assay, SNP(s) [rs115853233] 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

CFH

Gene Name

complement factor H

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000186.3		Intron			NP_000177.2
NM_001014975.2		Intron			NP_001014975.1
XM_017001108.1		Intron			XP_016856597.1

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