Variant (rsID / SNP)

rs371539613

rs371539613 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ILK. Location: chromosome 11, position 6,629,445. Clinical significance in the table: Likely benign.

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Reference-table entries

ILKLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:6629445
Cytoband: 11p15.4
HGVS: NM_006284.4(TAF10):c.*2707G>A
Allele change: Silent

Associated conditions / phenotypes

Primary familial hypertrophic cardiomyopathy

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.