Variants
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rs373175897

  • Uncertain significance

Your Genotype

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Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases did not allow this variant to be ruled in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.

Reference Allele

C


Alternative Allele

A

Chromosome

9


Location

110767913


Variant Type

SNP

Genes

ClinVar

Name

NM_005592.4(MUSK):c.1014C>A (p.Asn338Lys)


Allele

A


Clinical Significance

Uncertain significance

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