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Variant (rsID / SNP)

rs1560440

TBC1D9

rs1560440 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D9. Location: chromosome 4, position 141,543,997. The table records no clinical significance for this variant.

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Reference-table entries

TBC1D9Not classified
Variant type
synonymous_variant
Chromosome / position
4:141543997
HGVS
NM_015130.3,c.3153C>T,p.His1051His
Allele change
Synonymous_H1051H

Public references

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