Variant (rsID / SNP)

rs372870729

rs372870729 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK2. Location: chromosome 4, position 113,970,846. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ANK2Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 4:113970846
Cytoband: 4q25
HGVS: NM_001148.6(ANK2):c.-39G>T
Allele change: Silent

Associated conditions / phenotypes

Cardiac arrhythmia, ankyrin-B-related

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.