Variant (rsID / SNP)

rs61753726

rs61753726 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VPS13B. Location: chromosome 8, position 100,865,682. Clinical significance in the table: Benign.

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Reference-table entries

VPS13BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:100865682
Cytoband: 8q22.2
HGVS: NM_152564.5(VPS13B):c.10065G>T (p.Ala3355=)
Allele change: Synonymous_A3380A

Associated conditions / phenotypes

Cohen syndrome|History of neurodevelopmental disorder

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.