Variant (rsID / SNP)

rs201316362

rs201316362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SELENON. Location: chromosome 1, position 26,138,009. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SELENONUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:26138009
Cytoband: 1p36.11
HGVS: NM_020451.3(SELENON):c.1075A>G (p.Ile359Val)
Allele change: Missense_I325V

Associated conditions / phenotypes

Eichsfeld type congenital muscular dystrophy

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.