Variant (rsID / SNP)

rs143655258

rs143655258 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCARB2. Location: chromosome 4, position 77,100,807. Clinical significance in the table: Benign.

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Reference-table entries

SCARB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:77100807
Cytoband: 4q21.1
HGVS: NM_005506.4(SCARB2):c.475A>G (p.Met159Val)
Allele change: Silent

Associated conditions / phenotypes

Action myoclonus-renal failure syndrome|Seizure|Progressive myoclonic epilepsy

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.