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Variant (rsID / SNP)

rs200937358

SYNE2

rs200937358 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNE2. Location: chromosome 14, position 64,683,064. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SYNE2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
14:64683064
Cytoband
14q23.2
HGVS
NM_182914.3(SYNE2):c.19501C>T (p.Pro6501Ser)
Allele change
Missense_P6501S

Associated conditions / phenotypes

Emery-Dreifuss muscular dystrophy 5, autosomal dominant

Public references

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