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Variant (rsID / SNP)

rs768007208

FKRP

rs768007208 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FKRP. Location: chromosome 19, position 47,259,238. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FKRPConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
19:47259238
Cytoband
19q13.32
HGVS
NM_024301.5(FKRP):c.531G>A (p.Glu177=)
Allele change
Synonymous_E177E

Associated conditions / phenotypes

Walker-Warburg congenital muscular dystrophy|Autosomal recessive limb-girdle muscular dystrophy type 2I

Public references

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