Variant (rsID / SNP)

rs17106351

rs17106351 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR11H6. Location: chromosome 14, position 20,692,305. The table records no clinical significance for this variant.

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Reference-table entries

OR11H6Not classified

Variant type: missense_variant
Chromosome / position: 14:20692305
HGVS: NM_001004480.1,c.437G>A,p.Arg146His
Allele change: Missense_R146H

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.