Variant (rsID / SNP)

rs7830832

rs7830832 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TONSL. Location: chromosome 8, position 145,661,675. The table records no clinical significance for this variant.

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Reference-table entries

TONSLNot classified

Variant type: missense_variant
Chromosome / position: 8:145661675
HGVS: NM_013432.5,c.2141C>T,p.Ala714Val
Allele change: Missense_A714V

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.