Variant (rsID / SNP)

rs17261772

rs17261772 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAB3GAP1. Location: chromosome 2, position 135,911,422. Clinical significance in the table: Benign.

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Reference-table entries

RAB3GAP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:135911422
Cytoband: 2q21.3
HGVS: NM_012233.3(RAB3GAP1):c.2265T>C (p.Phe755=)
Allele change: Synonymous_F755F

Associated conditions / phenotypes

Warburg micro syndrome|Warburg micro syndrome 1|Martsolf syndrome 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.