Variant (rsID / SNP)

rs10404119

rs10404119 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR7A17. Location: chromosome 19, position 14,991,963. The table records no clinical significance for this variant.

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Reference-table entries

OR7A17Not classified

Variant type: missense_variant
Chromosome / position: 19:14991963
HGVS: NM_030901.2,c.205G>T,p.Ala69Ser
Allele change: Missense_A69S

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.