Variant (rsID / SNP)

rs17819466

rs17819466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNC. Location: chromosome 9, position 117,819,436. The table records no clinical significance for this variant.

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Reference-table entries

TNCNot classified

Variant type: synonymous_variant
Chromosome / position: 9:117819436
HGVS: NM_002160.4,c.4575G>A,p.Thr1525Thr
Allele change: Synonymous_T1525T

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.