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Variant (rsID / SNP)

rs1551886

ALDH3B2

rs1551886 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH3B2. Location: chromosome 11, position 67,430,762. The table records no clinical significance for this variant.

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Reference-table entries

ALDH3B2Not classified
Variant type
missense_variant
Chromosome / position
11:67430762
HGVS
NM_001031615.3,c.1082A>G,p.His361Arg
Allele change
Missense_H361R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.