List of variants in gene combination IL10, IL19 reported as uncertain significance for immune system disorder

Minimum submission review status:		Collection method:
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)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000572.3(IL10):c.225+6A>G	rs749041176	0.00008
NM_000572.3(IL10):c.371G>A (p.Arg124Gln)	rs201365412	0.00004
NM_000572.3(IL10):c.374G>A (p.Arg125His)	rs374619208	0.00003
NM_000572.3(IL10):c.365G>A (p.Arg122Lys)	rs371608920	0.00001
NM_000572.3(IL10):c.370C>T (p.Arg124Trp)	rs746523858	0.00001
NM_000572.3(IL10):c.209T>A (p.Leu70Ter)	rs1558603013
NM_000572.3(IL10):c.374G>T (p.Arg125Leu)	rs374619208
NM_000572.3(IL10):c.378+6T>C

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