Variant (rsID / SNP)

rs4639193

rs4639193 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CMYA5. Location: chromosome 5, position 79,030,045. The table records no clinical significance for this variant.

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Reference-table entries

CMYA5Not classified

Variant type: synonymous_variant
Chromosome / position: 5:79030045
HGVS: NM_153610.5,c.5457A>G,p.Val1819Val
Allele change: Synonymous_V1819V

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.