Variant (rsID / SNP)

rs184693266

rs184693266 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VPS13B. Location: chromosome 8, position 100,493,911. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

VPS13BBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 8:100493911
Cytoband: 8q22.2
HGVS: NM_152564.5(VPS13B):c.3751A>G (p.Thr1251Ala)
Allele change: Missense_T1251A

Associated conditions / phenotypes

Cohen syndrome

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.