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Variant (rsID / SNP)

rs1867380

AQP9

rs1867380 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AQP9. Location: chromosome 15, position 58,476,281. The table records no clinical significance for this variant.

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Reference-table entries

AQP9Not classified
Variant type
missense_variant
Chromosome / position
15:58476281
HGVS
NM_020980.5,c.835A>G,p.Thr279Ala
Allele change
Missense_T214A

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.