Variant (rsID / SNP)

rs139071237

rs139071237 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRWD3. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

BRWD3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Cytoband: Xq21.1
HGVS: NM_153252.5(BRWD3):c.33G>A (p.Glu11=)
Allele change: Synonymous_E11E

Associated conditions / phenotypes

Intellectual disability, X-linked 93|History of neurodevelopmental disorder

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.