Variant (rsID / SNP)

rs8178992

rs8178992 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHAT. Location: chromosome 10, position 50,863,147. Clinical significance in the table: Benign.

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Reference-table entries

CHATBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:50863147
Cytoband: 10q11.23
HGVS: NM_020549.5(CHAT):c.1641T>C (p.His547=)
Allele change: Synonymous_H429H

Associated conditions / phenotypes

Familial infantile myasthenia

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.