Related gene-specific medical variations for Gene (Select 89782) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2281233	NM_001136049.3(LMLN):c.1967G>C (p.Cys656Ser)	LMLN, LMLN-AS1 (C619S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 814517	GRCh37/hg19 3q29(chr3:197736816-197851986)x1	LMLN	Copy number loss	not provided	GUncertain significance
Select item 161526	NM_001136049.3(LMLN):c.1093G>T (p.Gly365Cys)	LMLN (G373C +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance

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