Variant (rsID / SNP)

rs796052455

rs796052455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXG1. Location: chromosome 14, position 29,236,861. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FOXG1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:29236861
Cytoband: 14q12
HGVS: NM_005249.5(FOXG1):c.376G>A (p.Gly126Ser)
Allele change: Missense_G126S

Associated conditions / phenotypes

Rett syndrome, congenital variant

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.