Variant (rsID / SNP)

rs2507941

rs2507941 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITGA9. Location: chromosome 3, position 37,536,056. 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: 3:37536056
Cytoband: 3p22.2
HGVS: NM_002207.3(ITGA9):c.609C>T (p.Thr203=)
Allele change: Synonymous_T203T

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.