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Variant (rsID / SNP)

rs3812111

COL10A1NT5DC1

rs3812111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL10A1, NT5DC1. Location: chromosome 6, position 116,443,735. The table records no clinical significance for this variant.

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Reference-table entries

COL10A1Not classified
Variant type
single nucleotide variant
Chromosome / position
6:116443735
Cytoband
6q22.1
HGVS
NM_000493.4(COL10A1):c.155-611A>T
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.