Related gene-specific medical variations for Gene (Select 11188) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3200234	NM_007184.4(NISCH):c.52G>A (p.Glu18Lys)	LOC129936862, NISCH (E18K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402047	NM_007184.4(NISCH):c.20T>C (p.Phe7Ser)	LOC129936862, NISCH (F7S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386578	NM_007184.4(NISCH):c.13C>G (p.Arg5Gly)	LOC129936862, NISCH (R5G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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