Variant (rsID / SNP)

rs56084453

rs56084453 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF502. Location: chromosome 3, position 44,762,830. The table records no clinical significance for this variant.

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Reference-table entries

ZNF502Not classified

Variant type: missense_variant
Chromosome / position: 3:44762830
HGVS: NM_001134440.2,c.521A>G,p.Gln174Arg
Allele change: Missense_Q174R

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.