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Variant (rsID / SNP)

rs267606627

ACTA1

rs267606627 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTA1. Location: chromosome 1, position 229,568,534. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

ACTA1Other
Clinical significance (as recorded)
no interpretation for the single variant
Variant type
single nucleotide variant
Chromosome / position
1:229568534
Cytoband
1q42.13
HGVS
NM_001100.4(ACTA1):c.223C>T (p.His75Tyr)
Allele change
Missense_H75Y

Public references

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