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Variant (rsID / SNP)

rs773385237

EFHC1

rs773385237 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EFHC1. Location: chromosome 6, position 52,344,502. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

EFHC1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
6:52344502
Cytoband
6p12.2
HGVS
NM_018100.4(EFHC1):c.1557C>T (p.Asn519=)
Allele change
Synonymous_N519N

Associated conditions / phenotypes

Juvenile myoclonic epilepsy|Juvenile myoclonic epilepsy|Typical absence seizure

Public references

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