Variant (rsID / SNP)

rs187796411

rs187796411 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ROBO2. Location: chromosome 3, position 77,623,752. Clinical significance in the table: Benign.

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Reference-table entries

ROBO2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:77623752
Cytoband: 3p12.3
HGVS: NM_001395656.1(ROBO2):c.2086C>T (p.Pro696Ser)
Allele change: Missense_P696S

Associated conditions / phenotypes

Vesicoureteral reflux 2

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.