Variant (rsID / SNP)

rs504280

rs504280 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF708. Location: chromosome 19, position 21,477,379. The table records no clinical significance for this variant.

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Reference-table entries

ZNF708Not classified

Variant type: missense_variant
Chromosome / position: 19:21477379
HGVS: NM_021269.3,c.389G>A,p.Arg130Gln
Allele change: Missense_R66Q

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.