Variant (rsID / SNP)

rs9565152

rs9565152 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D4. Location: chromosome 13, position 75,915,261. Clinical significance in the table: Likely benign.

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Reference-table entries

TBC1D4Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 13:75915261
Cytoband: 13q22.2
HGVS: NM_014832.5(TBC1D4):c.1611T>G (p.Ser537=)
Allele change: Synonymous_S537S

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.