Variant (rsID / SNP)

rs669

rs669 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to A2M. Location: chromosome 12, position 9,232,268. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

A2MBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:9232268
Cytoband: 12p13.31
HGVS: NM_000014.6(A2M):c.2998A>G (p.Ile1000Val)
Allele change: Missense_I1000V

Associated conditions / phenotypes

ALPHA-2-MACROGLOBULIN POLYMORPHISM

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.