Variant (rsID / SNP)

rs4746

rs4746 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLO1. Location: chromosome 6, position 38,650,628. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GLO1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 6:38650628
Cytoband: 6p21.2
HGVS: NM_006708.3(GLO1):c.332A>C (p.Glu111Ala)
Allele change: Missense_E111A

Associated conditions / phenotypes

Autism susceptibility 1

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.