Variant (rsID / SNP)

rs1126744

rs1126744 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGD1. Clinical significance in the table: Benign.

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Reference-table entries

FGD1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp11.22
HGVS: NM_004463.3(FGD1):c.2136A>G (p.Pro712=)
Allele change: Synonymous_P712P

Associated conditions / phenotypes

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.