Variant (rsID / SNP)

rs1851724

rs1851724 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR13C5. Location: chromosome 9, position 107,360,922. The table records no clinical significance for this variant.

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Reference-table entries

OR13C5Not classified

Variant type: missense_variant
Chromosome / position: 9:107360922
HGVS: NM_001004482.1,c.773T>C,p.Met258Thr
Allele change: Missense_M258T

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.