Variant (rsID / SNP)

rs1049467

rs1049467 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DAZAP2. Location: chromosome 12, position 51,636,259. The table records no clinical significance for this variant.

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Reference-table entries

DAZAP2Not classified

Variant type: synonymous_variant
Chromosome / position: 12:51636259
HGVS: NM_001136266.2,c.447C>T,p.Leu149Leu
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.