ClinVar Miner

List of variants in gene STAT5B reported as likely benign for Growth hormone insensitivity with immune dysregulation 1, autosomal recessive; Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012448.4(STAT5B):c.993G>A (p.Thr331=)	rs59491077	0.01527
NM_012448.4(STAT5B):c.2237+15T>C	rs113762956	0.01303

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