Variant (rsID / SNP)

rs149961458

rs149961458 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AUTS2. Location: chromosome 7, position 69,583,206. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

AUTS2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:69583206
Cytoband: 7q11.22
HGVS: NM_015570.4(AUTS2):c.611A>G (p.Glu204Gly)
Allele change: Missense_E204G

Associated conditions / phenotypes

Autism spectrum disorder due to AUTS2 deficiency

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.