Variant (rsID / SNP)

rs12980833

rs12980833 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR7E24. Location: chromosome 19, position 9,362,297. The table records no clinical significance for this variant.

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Reference-table entries

OR7E24Not classified

Variant type: missense_variant
Chromosome / position: 19:9362297
HGVS: NM_001079935.2,c.578C>T,p.Ser193Phe
Allele change: Missense_S193F

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.