Variant (rsID / SNP)

rs111663599

rs111663599 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLIN1. Location: chromosome 15, position 90,213,343. Clinical significance in the table: Benign.

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Reference-table entries

PLIN1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:90213343
Cytoband: 15q26.1
HGVS: NM_002666.5(PLIN1):c.466G>T (p.Val156Leu)
Allele change: Missense_V156L

Associated conditions / phenotypes

Monogenic diabetes

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.