Variant (rsID / SNP)

rs2297866

rs2297866 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANGPTL2, RALGPS1. Location: chromosome 9, position 129,854,199. The table records no clinical significance for this variant.

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Reference-table entries

ANGPTL2Not classified

Variant type: synonymous_variant
Chromosome / position: 9:129854199
HGVS: NM_012098.3,c.1032C>T,p.Asp344Asp
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.