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Variant (rsID / SNP)

rs2722722

ZNF112

rs2722722 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF112. Location: chromosome 19, position 44,832,875. The table records no clinical significance for this variant.

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Reference-table entries

ZNF112Not classified
Variant type
missense_variant
Chromosome / position
19:44832875
HGVS
NM_001348281.2,c.1504T>C,p.Tyr502His
Allele change
Missense_Y485H

Associated conditions / phenotypes

Missense_Y479H|Missense_Y479H

Public references

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