Related gene-specific medical variations for Gene (Select 142910) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3155517	NM_001031709.3(RNLS):c.55C>G (p.Leu19Val)	LIPJ, RNLS (L19V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2799241	NM_001031709.3(RNLS):c.32T>G (p.Met11Arg)	LIPJ, RNLS (M11R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1250700	NM_001031709.3(RNLS):c.111G>C (p.Glu37Asp)	LIPJ, LOC130004283 +1 more (E37D)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign

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