Variant (rsID / SNP)

rs5951308

rs5951308 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BTK. Clinical significance in the table: Benign.

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Reference-table entries

BTKBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq22.1
HGVS: NM_001287344.2(BTK):c.71A>G (p.Glu24Gly)
Allele change: Missense_E24G

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.