Variant (rsID / SNP)

rs2240228

rs2240228 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10H3. Location: chromosome 19, position 15,852,872. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

OR10H3Not classified

Variant type: missense_variant
Chromosome / position: 19:15852872
HGVS: NM_013938.2,c.670G>A,p.Val224Met
Allele change: Missense_V224M

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.