Variant (rsID / SNP)

rs115862064

rs115862064 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUBB2A. Location: chromosome 6, position 3,155,988. Clinical significance in the table: Benign.

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Reference-table entries

TUBB2ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:3155988
Cytoband: 6p25.2
HGVS: NM_001069.3(TUBB2A):c.167-19C>T
Allele change: Silent

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.