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Variant (rsID / SNP)

rs201405429

ROBO3

rs201405429 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ROBO3. Location: chromosome 11, position 124,744,752. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ROBO3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:124744752
Cytoband
11q24.2
HGVS
NM_022370.4(ROBO3):c.2020C>T (p.Arg674Cys)
Allele change
Missense_R674C

Associated conditions / phenotypes

Inborn genetic diseases|Gaze palsy, familial horizontal, with progressive scoliosis 1

Public references

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