Variant (rsID / SNP)

rs267733

rs267733 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANXA9. Location: chromosome 1, position 150,958,836. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ANXA9Not classified

Variant type: missense_variant
Chromosome / position: 1:150958836
HGVS: NM_003568.3,c.497A>G,p.Asp166Gly
Allele change: Missense_D166G

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.