Variant (rsID / SNP)

rs61737042

rs61737042 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHRNA4. Location: chromosome 20, position 61,981,710. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CHRNA4Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 20:61981710
Cytoband: 20q13.33
HGVS: NM_000744.7(CHRNA4):c.1053C>T (p.Ile351=)
Allele change: Synonymous_I351I

Associated conditions / phenotypes

Autosomal dominant nocturnal frontal lobe epilepsy|Seizure

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.