Variant (rsID / SNP)

rs2276326

rs2276326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GAR1. Location: chromosome 4, position 110,737,389. The table records no clinical significance for this variant.

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Reference-table entries

GAR1Not classified

Variant type: synonymous_variant
Chromosome / position: 4:110737389
HGVS: NM_018983.4,c.69T>C,p.Gly23Gly
Allele change: Synonymous_G23G

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.