Variant (rsID / SNP)

rs3803430

rs3803430 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH1A3. Location: chromosome 15, position 101,445,815. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ALDH1A3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:101445815
Cytoband: 15q26.3
HGVS: NM_000693.4(ALDH1A3):c.1156A>G (p.Met386Val)
Allele change: Missense_M279V

Associated conditions / phenotypes

Isolated microphthalmia 8

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.