Variants
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rs61747683

  • Benign

Your Genotype

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Description

Reference Allele

A


Alternative Allele

G

Chromosome

2


Location

219233429


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_018089.3(ANKZF1):c.815A>G (p.Tyr272Cys)


Allele

G


Clinical Significance

Benign

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