Variant (rsID / SNP)

rs16839515

rs16839515 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPHP3. Location: chromosome 3, position 132,409,455. Clinical significance in the table: Benign.

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Reference-table entries

NPHP3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:132409455
Cytoband: 3q22.1
HGVS: NM_153240.5(NPHP3):c.2610G>A (p.Pro870=)
Allele change: Silent

Associated conditions / phenotypes

Nephronophthisis|NPHP3-related Meckel-like syndrome|Renal-hepatic-pancreatic dysplasia 1|Nephronophthisis 3

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.