Related gene-specific medical variations for Gene (Select 59307) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2404079	NM_001135054.2(SIGIRR):c.830G>T (p.Arg277Leu)	LOC130005063, SIGIRR (R277L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389383	NM_001135054.2(SIGIRR):c.787G>T (p.Gly263Cys)	LOC130005063, SIGIRR (G263C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 756397	NM_001135054.2(SIGIRR):c.801C>T (p.Asp267=)	LOC130005063, SIGIRR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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