Variant (rsID / SNP)

rs41312114

rs41312114 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HDAC6. Clinical significance in the table: Likely benign.

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Reference-table entries

HDAC6Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Cytoband: Xp11.23
HGVS: NM_006044.4(HDAC6):c.3248G>A (p.Gly1083Asp)
Allele change: Missense_G1097D

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.