Variant (rsID / SNP)

rs12731843

rs12731843 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL11A1. Location: chromosome 1, position 103,491,461. Clinical significance in the table: Benign.

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Reference-table entries

COL11A1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:103491461
Cytoband: 1p21.1
HGVS: NM_001854.4(COL11A1):c.898-292A>C
Allele change: Silent

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.