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Variant (rsID / SNP)

rs6456880

ZNF311

rs6456880 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF311. Location: chromosome 6, position 28,963,248. The table records no clinical significance for this variant.

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Reference-table entries

ZNF311Not classified
Variant type
missense_variant
Chromosome / position
6:28963248
HGVS
NM_001010877.5,c.1531A>C,p.Lys511Gln
Allele change
Missense_K419Q

Public references

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