Variant (rsID / SNP)

rs77690058

rs77690058 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10X1. Location: chromosome 1, position 158,549,421. The table records no clinical significance for this variant.

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Reference-table entries

OR10X1Not classified

Variant type: missense_variant
Chromosome / position: 1:158549421
HGVS: NM_001004477.1,c.269C>T,p.Thr90Met
Allele change: Missense_T90M

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.