Variant (rsID / SNP)

rs11015859

rs11015859 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAB18. Location: chromosome 10, position 27,826,951. Clinical significance in the table: Benign.

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Reference-table entries

RAB18Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:27826951
Cytoband: 10p12.1
HGVS: NM_021252.5(RAB18):c.592G>A (p.Ala198Thr)
Allele change: Missense_A227T

Associated conditions / phenotypes

Warburg micro syndrome 3

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.