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Variant (rsID / SNP)

rs188582283

ROBO2

rs188582283 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ROBO2. Location: chromosome 3, position 77,629,200. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ROBO2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
3:77629200
Cytoband
3p12.3
HGVS
NM_001395656.1(ROBO2):c.2443C>T (p.Arg815Trp)
Allele change
Missense_R815W

Associated conditions / phenotypes

Vesicoureteral reflux 2|Congenital anomaly of kidney and urinary tract

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.