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Variant (rsID / SNP)

rs200131009

ROBO2

rs200131009 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ROBO2. Location: chromosome 3, position 77,684,117. 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
3:77684117
Cytoband
3p12.3
HGVS
NM_001395656.1(ROBO2):c.3869G>T (p.Arg1290Leu)
Allele change
Missense_R1290L

Associated conditions / phenotypes

Vesicoureteral reflux 2

Public references

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