Variant (rsID / SNP)

rs2292927

rs2292927 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL22A1. Location: chromosome 8, position 139,838,912. The table records no clinical significance for this variant.

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Reference-table entries

COL22A1Not classified

Variant type: missense_variant
Chromosome / position: 8:139838912
HGVS: NM_152888.3,c.958A>G,p.Ser320Gly
Allele change: Missense_S320G

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.