Variant (rsID / SNP)

rs7719091

rs7719091 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH7A1. Location: chromosome 5, position 125,882,138. Clinical significance in the table: Likely benign.

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Reference-table entries

ALDH7A1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:125882138
Cytoband: 5q23.2
HGVS: NM_001182.5(ALDH7A1):c.1490-47A>G
Allele change: Silent

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.