Variant (rsID / SNP)

rs2073478

rs2073478 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH1B1. Location: chromosome 9, position 38,396,065. Clinical significance in the table: Benign.

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Reference-table entries

ALDH1B1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:38396065
Cytoband: 9p13.1
HGVS: NM_000692.5(ALDH1B1):c.320G>T (p.Arg107Leu)
Allele change: Missense_R107L

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.