Variant (rsID / SNP)

rs79341122

rs79341122 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD1. Location: chromosome 10, position 92,680,801. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ANKRD1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:92680801
Cytoband: 10q23.31
HGVS: NM_014391.3(ANKRD1):c.-17A>G
Allele change: Silent

Associated conditions / phenotypes

Primary dilated cardiomyopathy|Congenital total pulmonary venous return anomaly

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.