IthaID: 3525



Names and Sequences

Functionality: Disease modifying mutation Pathogenicity: N/A
Common Name: rs3729569 HGVS Name: NG_008958.1:g.35707C>A

Context nucleotide sequence:
ACGCTTCCTACCCTTAACTGCTTTA [C>A] CATGCTATTCAAAGTTTTATCACCCT (Strand: -)

Also known as:

Comments: SNP associated with a higher white blood cell count in the Kore Association Resource (KARE) project of the Korean Genome Epidemiology Study (KoGES; n=8842). The association was replicated in healthy samples from the Cardio Vascular Disease Association Study (CAVAS) of KoGES (n=3667).

We follow the HGVS sequence variant nomenclature and IUPAC standards.

External Links

Phenotype

Allele Phenotype (Cis):N/A
Allele Phenotype (Trans):N/A
Associated Phenotypes: Abnormal white blood cell count [HP:0011893]

Location

Chromosome: 2
Locus: NG_008958.1
Locus Location: 35707
Size: 1 bp
Located at: MCM6
Specific Location: Intron 15

Other details

Type of Mutation: Point-Mutation(Substitution)
Effect on Gene/Protein Function: N/A
Ethnic Origin: Korean
Molecular mechanism: N/A
Inheritance: Quantitative trait
DNA Sequence Determined: Yes

In silico pathogenicity prediction

Sequence Viewer

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Publications / Origin

  1. Kim YK, Oh JH, Kim YJ, Hwang MY, Moon S, Low SK, Takahashi A, Matsuda K, Kubo M, Lee J, Kim BJ, Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach., Biomed Res Int , 2015(0), 914965, 2015 PubMed
Created on 2019-12-10 09:19:17, Last reviewed on (Show full history)

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