Variant (rsID / SNP)

rs74127323

rs74127323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAB18. Location: chromosome 10, position 27,793,279. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RAB18Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:27793279
Cytoband: 10p12.1
HGVS: NM_021252.5(RAB18):c.-20C>T
Allele change: Silent

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.