Variant (rsID / SNP)

rs7079481

rs7079481 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,959,242. Clinical significance in the table: Benign.

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Reference-table entries

MYPNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:69959242
Cytoband: 10q21.3
HGVS: NM_032578.4(MYPN):c.3403C>A (p.Pro1135Thr)
Allele change: Silent

Associated conditions / phenotypes

Cardiovascular phenotype|Dilated cardiomyopathy 1KK|MYPN-related myopathy

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.