Variant (rsID / SNP)

rs4878199

rs4878199 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH1B1. Location: chromosome 9, position 38,396,502. 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: 9:38396502
Cytoband: 9p13.1
HGVS: NM_000692.5(ALDH1B1):c.757G>A (p.Val253Met)
Allele change: Missense_V253M

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.