C0020538[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1338787	NM_173598.6(KSR2):c.2512C>T (p.Arg838Cys)	KSR2 (R838C)	Single nucleotide variant (missense variant)	Class III obesity +5 more	GUncertain significance
Select item 374097	NM_001009944.3(PKD1):c.8311G>A (p.Glu2771Lys)	PKD1 (E2771K)	Single nucleotide variant (missense variant)	not provided +4 more	GPathogenic/Likely pathogenic
Select item 24455	NM_033380.3(COL4A5):c.1871G>A (p.Gly624Asp)	COL4A5 (G624D)	Single nucleotide variant (missense variant)	COL4A5-related disorder +5 more	GPathogenic/Likely pathogenic

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