Variant (rsID / SNP)

rs2243563

rs2243563 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF853. Location: chromosome 7, position 6,656,830. The table records no clinical significance for this variant.

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Reference-table entries

ZNF853Not classified

Variant type: missense_variant
Chromosome / position: 7:6656830
HGVS: NM_017560.3,c.22G>A,p.Gly8Arg
Allele change: Missense_G8R

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.