Variants
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rs77280560

  • Benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

2


Location

219235490


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_018089.3(ANKZF1):c.1708C>T (p.Pro570Ser)


Allele

T


Clinical Significance

Benign

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