Variant (rsID / SNP)

rs6685323

rs6685323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AQP10. Location: chromosome 1, position 154,295,592. The table records no clinical significance for this variant.

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Reference-table entries

AQP10Not classified

Variant type: missense_variant
Chromosome / position: 1:154295592
HGVS: NM_080429.3,c.367C>T,p.His123Tyr
Allele change: Missense_H123Y

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.