Variant (rsID / SNP)

rs2602016

rs2602016 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC23. Location: chromosome 15, position 99,715,352. The table records no clinical significance for this variant.

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Reference-table entries

TTC23Not classified

Variant type: synonymous_variant
Chromosome / position: 15:99715352
HGVS: NM_001288615.3,c.768T>C,p.Leu256Leu
Allele change: Silent

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.