Variant (rsID / SNP)

rs7246969

rs7246969 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR7G1. Location: chromosome 19, position 9,225,940. The table records no clinical significance for this variant.

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Reference-table entries

OR7G1Not classified

Variant type: missense_variant
Chromosome / position: 19:9225940
HGVS: NM_001005192.2,c.500C>T,p.Ser167Phe
Allele change: Missense_S167F

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.