Variant (rsID / SNP)

rs16930998

rs16930998 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR51I1, OR51B5. Location: chromosome 11, position 5,462,702. The table records no clinical significance for this variant.

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Reference-table entries

OR51I1Not classified

Variant type: stop_gained
Chromosome / position: 11:5462702
HGVS: NM_001005288.3,c.43C>T,p.Gln15*
Allele change: Silent

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.