Variant (rsID / SNP)

rs2232434

rs2232434 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZSCAN12. Location: chromosome 6, position 28,358,893. The table records no clinical significance for this variant.

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Reference-table entries

ZSCAN12Not classified

Variant type: missense_variant
Chromosome / position: 6:28358893
HGVS: NM_001163391.2,c.1174A>G,p.Asn392Asp
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.