Variant (rsID / SNP)

rs794728019

rs794728019 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTA2. Location: chromosome 10, position 90,708,687. Clinical significance in the table: Uncertain significance.

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Reference-table entries

ACTA2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:90708687
Cytoband: 10q23.31
HGVS: NM_001613.4(ACTA2):c.1A>G (p.Met1Val)
Allele change: Missense_M1V

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.