List of variants in gene IL10 reported as uncertain significance for Inflammatory bowel disease

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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)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000572.3(IL10):c.530G>A (p.Arg177Gln)	rs376415487	0.00009
NM_000572.3(IL10):c.383G>T (p.Arg128Leu)	rs760677075	0.00001
NM_000572.3(IL10):c.434C>T (p.Ala145Val)	rs774072665	0.00001
NM_000572.3(IL10):c.444+6C>T	rs749664677	0.00001
NM_000572.3(IL10):c.514A>G (p.Met172Val)	rs768418064	0.00001
NM_000572.3(IL10):c.521T>C (p.Met174Thr)	rs762496248	0.00001
NM_000572.3(IL10):c.383G>A (p.Arg128Gln)	rs760677075
NM_000572.3(IL10):c.386T>A (p.Phe129Tyr)
NM_000572.3(IL10):c.424G>C (p.Val142Leu)
NM_000572.3(IL10):c.443A>G (p.Lys148Arg)
NM_000572.3(IL10):c.502A>G (p.Ile168Val)	rs2102436707
NM_000572.3(IL10):c.503T>A (p.Ile168Lys)
NM_000572.3(IL10):c.507A>C (p.Glu169Asp)	rs568879359
NM_000572.3(IL10):c.529C>T (p.Arg177Ter)
NM_000572.3(IL10):c.534C>A (p.Asn178Lys)
NM_000572.3(IL10):c.534C>G (p.Asn178Lys)	rs771277922

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