Variant (rsID / SNP)

rs2289037

rs2289037 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZSCAN30, ZNF397. Location: chromosome 18, position 32,834,095. The table records no clinical significance for this variant.

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Reference-table entries

ZSCAN30Not classified

Variant type: synonymous_variant
Chromosome / position: 18:32834095
HGVS: NM_001112734.4,c.804A>G,p.Thr268Thr
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.