List of variants in gene combination IL10, IL19 reported as likely benign for Inflammatory bowel disease

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000572.3(IL10):c.225+18G>A	rs376490444	0.00033
NM_000572.3(IL10):c.225+15G>A	rs1342823726	0.00002
NM_000572.3(IL10):c.225+17G>A	rs1674832645	0.00001
NM_000572.3(IL10):c.166-19C>T
NM_000572.3(IL10):c.166-7C>T
NM_000572.3(IL10):c.201G>A (p.Lys67=)	rs2102439750
NM_000572.3(IL10):c.213G>T (p.Leu71=)
NM_000572.3(IL10):c.225+20G>A
NM_000572.3(IL10):c.361C>T (p.Leu121=)
NM_000572.3(IL10):c.372G>A (p.Arg124=)
NM_000572.3(IL10):c.375C>A (p.Arg125=)	rs755403362
NM_000572.3(IL10):c.378+15A>C
NM_000572.3(IL10):c.378+16G>C
NM_000572.3(IL10):c.378+19_378+20delinsCC	rs2102439038

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