Variant (rsID / SNP)

rs7132431

rs7132431 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR6C1. Location: chromosome 12, position 55,714,772. The table records no clinical significance for this variant.

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Reference-table entries

OR6C1Not classified

Variant type: missense_variant
Chromosome / position: 12:55714772
HGVS: NM_001005182.2,c.389G>A,p.Cys130Tyr
Allele change: Missense_C130Y

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.