Variant (rsID / SNP)

rs79435376

rs79435376 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRIQ3. Location: chromosome 1, position 74,506,942. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LRRIQ3Not classified

Variant type: missense_variant
Chromosome / position: 1:74506942
HGVS: NM_001105659.2,c.1673C>T,p.Ala558Val
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.