Variant (rsID / SNP)

rs1909261

rs1909261 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR51B5, OR51J1. Location: chromosome 11, position 5,424,125. The table records no clinical significance for this variant.

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Reference-table entries

OR51B5Not classified

Variant type: intron_variant
Chromosome / position: 11:5424125
HGVS: NM_001005567.3,c.-359-55985C>T
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.