Variant (rsID / SNP)

rs140772352

rs140772352 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALAS2. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ALAS2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Cytoband: Xp11.21
HGVS: NM_000032.4(ALAS2):c.-258C>G

Associated conditions / phenotypes

X-linked sideroblastic anemia 1

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.