Related gene-specific medical variations for Gene (Select 386653) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2608419	NM_001014336.2(IL31):c.202T>C (p.Tyr68His)	IL31, LRRC43 (Y68H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2559676	NM_001014336.2(IL31):c.293T>C (p.Leu98Pro)	IL31, LRRC43 (L98P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2366827	NM_001014336.2(IL31):c.355G>A (p.Ala119Thr)	IL31, LRRC43 (A119T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2308644	NM_001014336.2(IL31):c.319A>G (p.Ile107Val)	IL31, LRRC43 (I107V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2301574	NM_001014336.2(IL31):c.101C>G (p.Pro34Arg)	IL31, LRRC43 (P34R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2248964	NM_001014336.2(IL31):c.376G>A (p.Val126Met)	IL31, LRRC43 (V126M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2244453	NM_001014336.2(IL31):c.297C>A (p.Asp99Glu)	IL31, LRRC43 (D99E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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