Variant (rsID / SNP)

rs141514527

rs141514527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZC3H4. Location: chromosome 19, position 47,570,343. The table records no clinical significance for this variant.

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Reference-table entries

ZC3H4Not classified

Variant type: missense_variant
Chromosome / position: 19:47570343
HGVS: NM_015168.2,c.3182C>T,p.Ala1061Val
Allele change: Missense_A1061V

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.