Variant (rsID / SNP)

rs2230265

rs2230265 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGD1. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FGD1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp11.22
HGVS: NM_004463.3(FGD1):c.*36C>T
Allele change: Silent

Associated conditions / phenotypes

Aarskog syndrome

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.