Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs7874348

OLFML2A

rs7874348 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OLFML2A. Location: chromosome 9, position 127,566,378. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

OLFML2ANot classified
Variant type
missense_variant
Chromosome / position
9:127566378
HGVS
NM_182487.4,c.925A>G,p.Thr309Ala
Allele change
Missense_T309A

Associated conditions / phenotypes

Chiari Malformation Type I|Chiari Malformation

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.