Variant (rsID / SNP)

rs2190686

rs2190686 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR7A5. Location: chromosome 19, position 14,938,616. The table records no clinical significance for this variant.

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Reference-table entries

OR7A5Not classified

Variant type: synonymous_variant
Chromosome / position: 19:14938616
HGVS: NM_001370480.1,c.438A>G,p.Leu146Leu
Allele change: Synonymous_L146L

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.