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Variant (rsID / SNP)

rs115155934

FKTN

rs115155934 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FKTN. Location: chromosome 9, position 108,402,370. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FKTNConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
9:108402370
Cytoband
9q31.2
HGVS
NM_001079802.2(FKTN):c.*4825T>C
Allele change
Silent

Associated conditions / phenotypes

Dilated cardiomyopathy 1X|Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.