ClinVar Miner

List of variants in gene PLIN1 reported as benign for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_002666.5(PLIN1):c.466G>T (p.Val156Leu) rs111663599 0.01084
NM_002666.5(PLIN1):c.692G>T (p.Arg231Leu) rs114583540 0.00826
NM_002666.5(PLIN1):c.812C>T (p.Ala271Val) rs58361219 0.00633
NM_002666.5(PLIN1):c.1139C>T (p.Ala380Val) rs146385147 0.00628
NM_002666.5(PLIN1):c.1043C>T (p.Ser348Leu) rs8179071 0.00586

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