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Variant (rsID / SNP)

rs749671

ZNF646

rs749671 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF646. Location: chromosome 16, position 31,088,347. The table records no clinical significance for this variant.

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Reference-table entries

ZNF646Not classified
Variant type
synonymous_variant
Chromosome / position
16:31088347
HGVS
NM_014699.4,c.702G>A,p.Glu234Glu
Allele change
Synonymous_E234E

Public references

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