ClinVar for MedGen (Select 382527) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1572045	NM_173842.3(IL1RN):c.300G>A (p.Glu100=)	IL1RN	Single nucleotide variant (synonymous variant)	Sterile multifocal osteomyelitis with periostitis and pustulosis +2 more	GLikely benign
Select item 1015756	NM_173842.3(IL1RN):c.212T>C (p.Ile71Thr)	IL1RN (I37T +3 more)	Single nucleotide variant (missense variant)	Gastric cancer +2 more	GUncertain significance
Select item 944477	NM_173842.3(IL1RN):c.496G>A (p.Val166Ile)	IL1RN (V166I +3 more)	Single nucleotide variant (missense variant)	Gastric cancer +2 more	GUncertain significance
Select item 827981	NM_173842.3(IL1RN):c.68C>T (p.Thr23Met)	IL1RN (T23M +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +3 more	GUncertain significance
Select item 330823	NM_173842.3(IL1RN):c.69G>A (p.Thr23=)	IL1RN	Single nucleotide variant (synonymous variant +1 more)	not provided +5 more	GBenign/Likely benign
Select item 14674	NM_173842.3(IL1RN):c.206-516ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC[2]	IL1RN	Microsatellite (intron variant)	Gastric cancer susceptibility after h. pylori infection +1 more	GPathogenic; risk factor

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