Variant (rsID / SNP)

rs104894338

rs104894338 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AQP2. Location: chromosome 12, position 50,344,912. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

AQP2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 12:50344912
Cytoband: 12q13.12
HGVS: NM_000486.6(AQP2):c.299G>T (p.Gly100Val)
Allele change: Missense_G100V

Associated conditions / phenotypes

Diabetes insipidus, nephrogenic, autosomal

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.