Variant (rsID / SNP)

rs267561

rs267561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITGA9. Location: chromosome 3, position 37,574,951. Clinical significance in the table: Benign.

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Reference-table entries

ITGA9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:37574951
Cytoband: 3p22.2
HGVS: NM_002207.3(ITGA9):c.1520G>A (p.Gly507Glu)
Allele change: Missense_G507E

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.