Variant (rsID / SNP)

rs36105360

rs36105360 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNB1. Location: chromosome 5, position 126,161,690. Clinical significance in the table: Benign.

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Reference-table entries

LMNB1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:126161690
Cytoband: 5q23.2
HGVS: NM_005573.4(LMNB1):c.1502C>T (p.Ala501Val)
Allele change: Missense_A501V

Associated conditions / phenotypes

Adult-onset autosomal dominant demyelinating leukodystrophy

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.