Variant (rsID / SNP)

rs2072164

rs2072164 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2F1. Location: chromosome 7, position 143,657,427. The table records no clinical significance for this variant.

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Reference-table entries

OR2F1Not classified

Variant type: missense_variant
Chromosome / position: 7:143657427
HGVS: NM_012369.3,c.364C>T,p.Arg122Cys
Allele change: Missense_R122C

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.