Variant (rsID / SNP)

rs151129325

rs151129325 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL9A1. Location: chromosome 6, position 70,990,715. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

COL9A1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:70990715
Cytoband: 6q13
HGVS: NM_001851.6(COL9A1):c.904G>A (p.Gly302Ser)
Allele change: Missense_G59S

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.