Variant (rsID / SNP)

rs2071126

rs2071126 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AVPR2. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

AVPR2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_000054.7(AVPR2):c.35G>A (p.Gly12Glu)
Allele change: Silent

Associated conditions / phenotypes

Diabetes insipidus, nephrogenic, X-linked

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.