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Variant (rsID / SNP)

rs7556176

MYOM3

rs7556176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYOM3. Location: chromosome 1, position 24,418,768. The table records no clinical significance for this variant.

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Reference-table entries

MYOM3Not classified
Variant type
synonymous_variant
Chromosome / position
1:24418768
HGVS
NM_152372.4,c.1128A>G,p.Pro376Pro
Allele change
Synonymous_P376P

Public references

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