Product Details

SNP ID

rs557626

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:49780117 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACGAGGTAGTAACAGTGGGGTGTGT[A/G]AGGATGCATCAGCACACATGATGGG

Phenotype

MIM: 611108

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

VWC2 PubMed Links

Gene Details

Gene

VWC2

Gene Name

von Willebrand factor C domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198570.4		Intron			NP_940972.2

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