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Variant (rsID / SNP)

rs6515646

TMC2

rs6515646 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMC2. Location: chromosome 20, position 2,593,863. The table records no clinical significance for this variant.

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Reference-table entries

TMC2Not classified
Variant type
synonymous_variant
Chromosome / position
20:2593863
HGVS
NM_080751.3,c.1767T>C,p.Ser589Ser
Allele change
Synonymous_S589S

Public references

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