Variant (rsID / SNP)

rs11084940

rs11084940 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNB2. Location: chromosome 19, position 2,433,890. Clinical significance in the table: Benign.

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Reference-table entries

LMNB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:2433890
Cytoband: 19p13.3
HGVS: NM_032737.4(LMNB2):c.1416T>C (p.Gly472=)
Allele change: Synonymous_G472G

Associated conditions / phenotypes

Lipodystrophy, partial, acquired, susceptibility to|Progressive myoclonic epilepsy type 9

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.