Variant (rsID / SNP)

rs10410943

rs10410943 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTL9. Location: chromosome 19, position 8,808,900. The table records no clinical significance for this variant.

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Reference-table entries

ACTL9Not classified

Variant type: missense_variant
Chromosome / position: 19:8808900
HGVS: NM_178525.5,c.152T>C,p.Val51Ala
Allele change: Missense_V51A

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.