Variant (rsID / SNP)

rs4625

rs4625 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DAG1. Location: chromosome 3, position 49,572,140. The table records no clinical significance for this variant.

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Reference-table entries

DAG1Not classified

Variant type: single nucleotide variant
Chromosome / position: 3:49572140
Cytoband: 3p21.31
HGVS: NM_004393.6(DAG1):c.*1508A>G
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.