Variant (rsID / SNP)

rs4649175

rs4649175 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYOM3. Location: chromosome 1, position 24,406,647. The table records no clinical significance for this variant.

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Reference-table entries

MYOM3Not classified

Variant type: synonymous_variant
Chromosome / position: 1:24406647
HGVS: NM_152372.4,c.2445C>T,p.Ala815Ala
Allele change: Synonymous_A815A

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.