Variant (rsID / SNP)

rs36088178

rs36088178 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D20. Location: chromosome 20, position 428,553. Clinical significance in the table: Benign.

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Reference-table entries

TBC1D20Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:428553
Cytoband: 20p13
HGVS: NM_144628.4(TBC1D20):c.236A>G (p.Asn79Ser)
Allele change: Missense_N79S

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.