Variant (rsID / SNP)

rs11579482

rs11579482 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COLGALT2. Location: chromosome 1, position 183,947,633. The table records no clinical significance for this variant.

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Reference-table entries

COLGALT2Not classified

Variant type: synonymous_variant
Chromosome / position: 1:183947633
HGVS: NM_015101.4,c.285G>T,p.Val95Val
Allele change: Synonymous_V95V

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.