Variant (rsID / SNP)

rs4646626

rs4646626 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH1A2. Location: chromosome 15, position 58,256,127. The table records no clinical significance for this variant.

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Reference-table entries

ALDH1A2Not classified

Variant type: missense_variant
Chromosome / position: 15:58256127
HGVS: NM_003888.4,c.1042G>A,p.Val348Ile
Allele change: Missense_V348I

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.