Variant (rsID / SNP)

rs2317676

rs2317676 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITGB3. Location: chromosome 17, position 45,388,283. Clinical significance in the table: Benign.

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Reference-table entries

ITGB3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:45388283
Cytoband: 17q21.32
HGVS: NM_000212.3(ITGB3):c.*713A>G
Allele change: Silent

Associated conditions / phenotypes

Glanzmann thrombasthenia

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.