Variant (rsID / SNP)

rs73141283

rs73141283 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2M5. Location: chromosome 1, position 248,309,356. The table records no clinical significance for this variant.

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Reference-table entries

OR2M5Not classified

Variant type: missense_variant
Chromosome / position: 1:248309356
HGVS: NM_001004690.1,c.907A>G,p.Lys303Glu
Allele change: Missense_K303E

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.