Variant (rsID / SNP)

rs11544484

rs11544484 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TOP1MT. Location: chromosome 8, position 144,406,705. The table records no clinical significance for this variant.

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Reference-table entries

TOP1MTNot classified

Variant type: missense_variant
Chromosome / position: 8:144406705
HGVS: NM_052963.3,c.766G>A,p.Val256Ile
Allele change: Missense_V158I

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.