Variant (rsID / SNP)

rs193922112

rs193922112 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AVPR2. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

AVPR2Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_000054.7(AVPR2):c.176T>C (p.Leu59Pro)
Allele change: Silent

Associated conditions / phenotypes

Nephrogenic diabetes insipidus

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.