Variants
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rs144301422

  • Benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

15


Location

31031122


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001252024.2(TRPM1):c.2988G>A (p.Leu996=)


Allele

T


Clinical Significance

Benign

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