List of variants in gene combination IL10, IL19, LOC129932369 reported as likely benign for Inflammatory bowel disease

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000572.3(IL10):c.345C>T (p.Asn115=)	rs5743626	0.00073
NM_000572.3(IL10):c.228T>C (p.Gly76=)	rs139352858	0.00004
NM_000572.3(IL10):c.309A>G (p.Pro103=)	rs987614203	0.00004
NM_000572.3(IL10):c.321G>A (p.Ala107=)	rs560908141	0.00003
NM_000572.3(IL10):c.255G>A (p.Glu85=)	rs769682299	0.00001
NM_000572.3(IL10):c.297G>A (p.Glu99=)	rs1220388430	0.00001
NM_000572.3(IL10):c.336G>C (p.Leu112=)	rs767727378	0.00001
NM_000572.3(IL10):c.252T>G (p.Ser84=)
NM_000572.3(IL10):c.261C>T (p.Ile87=)
NM_000572.3(IL10):c.273G>A (p.Leu91=)	rs1674815134
NM_000572.3(IL10):c.276G>A (p.Glu92=)	rs1674814817
NM_000572.3(IL10):c.327G>A (p.Val109=)
NM_000572.3(IL10):c.334C>T (p.Leu112=)	rs2102439153

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