Variant (rsID / SNP)

rs113902159

rs113902159 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPHP4. Location: chromosome 1, position 6,038,319. Clinical significance in the table: Benign.

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Reference-table entries

NPHP4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:6038319
Cytoband: 1p36.31
HGVS: NM_015102.5(NPHP4):c.279+11G>A
Allele change: Silent

Associated conditions / phenotypes

Nephronophthisis 4|Senior-Loken syndrome 4|Nephronophthisis

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.