Variant (rsID / SNP)

rs1329957

rs1329957 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR1Q1. Location: chromosome 9, position 125,377,505. The table records no clinical significance for this variant.

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Reference-table entries

OR1Q1Not classified

Variant type: missense_variant
Chromosome / position: 9:125377505
HGVS: NM_012364.1,c.489A>G,p.Ile163Met
Allele change: Missense_I163M

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.