Variant (rsID / SNP)

rs371940910

rs371940910 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTC1. Location: chromosome 15, position 35,084,343. Clinical significance in the table: Uncertain significance.

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Reference-table entries

ACTC1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:35084343
Cytoband: 15q14
HGVS: NM_005159.5(ACTC1):c.756T>G (p.Ile252Met)
Allele change: Silent

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.