Variant (rsID / SNP)

rs11595587

rs11595587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAT1A. Location: chromosome 10, position 82,049,332. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MAT1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:82049332
Cytoband: 10q22.3
HGVS: NM_000429.3(MAT1A):c.-153C>T
Allele change: Silent

Associated conditions / phenotypes

Hepatic methionine adenosyltransferase deficiency

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.