Variant (rsID / SNP)

rs62577237

rs62577237 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INVS, ERP44. Location: chromosome 9, position 102,861,568. Clinical significance in the table: Likely benign.

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Reference-table entries

INVSLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:102861568
Cytoband: 9q31.1
HGVS: NM_014425.5(INVS):c.-155C>T
Allele change: Silent

Associated conditions / phenotypes

Infantile 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.