Variant (rsID / SNP)

rs34768413

rs34768413 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GATAD1. Location: chromosome 7, position 92,085,763. Clinical significance in the table: Benign.

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Reference-table entries

GATAD1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:92085763
Cytoband: 7q21.2
HGVS: NM_021167.5(GATAD1):c.697C>T (p.Arg233Trp)
Allele change: Silent

Associated conditions / phenotypes

Dilated cardiomyopathy 2B

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.