Variant (rsID / SNP)

rs10414255

rs10414255 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR7G3. Location: chromosome 19, position 9,237,542. The table records no clinical significance for this variant.

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Reference-table entries

OR7G3Not classified

Variant type: missense_variant
Chromosome / position: 19:9237542
HGVS: NM_001001958.1,c.85A>G,p.Met29Val
Allele change: Missense_M29V

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.