Variant (rsID / SNP)

rs1046677

rs1046677 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTR8. Location: chromosome 3, position 53,905,308. The table records no clinical significance for this variant.

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Reference-table entries

ACTR8Not classified

Variant type: synonymous_variant
Chromosome / position: 3:53905308
HGVS: NM_022899.5,c.1518A>G,p.Gly506Gly
Allele change: Synonymous_G506G

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.