Variant (rsID / SNP)

rs680055

rs680055 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP3A43. Location: chromosome 7, position 99,457,605. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CYP3A43Not classified

Variant type: missense_variant
Chromosome / position: 7:99457605
HGVS: NM_022820.5,c.1018C>G,p.Pro340Ala
Allele change: Missense_P340A

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.