Variant (rsID / SNP)

rs2072165

rs2072165 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2F1. Location: chromosome 7, position 143,657,473. The table records no clinical significance for this variant.

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Reference-table entries

OR2F1Not classified

Variant type: missense_variant
Chromosome / position: 7:143657473
HGVS: NM_012369.3,c.410A>G,p.His137Arg
Allele change: Missense_H137R

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.