Variant (rsID / SNP)

rs10407547

rs10407547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF577. Location: chromosome 19, position 52,376,126. The table records no clinical significance for this variant.

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Reference-table entries

ZNF577Not classified

Variant type: missense_variant
Chromosome / position: 19:52376126
HGVS: NM_001370447.1,c.1117G>A,p.Glu373Lys
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.