Product Details

SNP ID

rs2873966

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:66215855 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAATGGGAGAGACCATTGAGATAC[A/G]GAAAAAGTAGGAATAGTTCCTGCCT

Phenotype

MIM: 138700

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

APOH PubMed Links

Gene Details

Gene

APOH

Gene Name

apolipoprotein H

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000042.2		Intron			NP_000033.2

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