Variant (rsID / SNP)

rs1345658

rs1345658 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF30. Location: chromosome 19, position 35,435,006. The table records no clinical significance for this variant.

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Reference-table entries

ZNF30Not classified

Variant type: missense_variant
Chromosome / position: 19:35435006
HGVS: NM_001099437.2,c.1139G>A,p.Arg380Lys
Allele change: Missense_R379K

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.