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Variant (rsID / SNP)

rs10871453

ZNF768

rs10871453 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF768. Location: chromosome 16, position 30,536,918. The table records no clinical significance for this variant.

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Reference-table entries

ZNF768Not classified
Variant type
missense_variant
Chromosome / position
16:30536918
HGVS
NM_024671.4,c.543G>C,p.Glu181Asp
Allele change
Missense_E181D

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.