Variant (rsID / SNP)

rs3809482

rs3809482 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZSCAN29, TUBGCP4. Location: chromosome 15, position 43,661,802. The table records no clinical significance for this variant.

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Reference-table entries

ZSCAN29Not classified

Variant type: missense_variant
Chromosome / position: 15:43661802
HGVS: NM_001372080.1,c.310A>G,p.Arg104Gly
Allele change: Missense_R104G

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.