Variant (rsID / SNP)

rs7522034

rs7522034 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANP32E. Location: chromosome 1, position 150,199,123. The table records no clinical significance for this variant.

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Reference-table entries

ANP32ENot classified

Variant type: missense_variant
Chromosome / position: 1:150199123
HGVS: NM_001280560.2,c.332C>A,p.Ala111Glu
Allele change: Missense_A111E

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.