Related gene-specific medical variations for Gene (Select 401036) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2623577	NM_212556.4(ASB18):c.1173G>C (p.Leu391Phe)	ASB18, GBX2-AS1 (L391F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455966	NM_212556.4(ASB18):c.1297C>T (p.Arg433Cys)	ASB18, GBX2-AS1 (R433C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370793	NM_212556.4(ASB18):c.1195A>G (p.Ile399Val)	ASB18, GBX2-AS1 (I399V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343721	NM_212556.4(ASB18):c.1300A>G (p.Arg434Gly)	ASB18, GBX2-AS1 (R434G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296831	NM_212556.4(ASB18):c.1385A>G (p.Gln462Arg)	ASB18, GBX2-AS1 (Q462R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294238	NM_212556.4(ASB18):c.1238C>T (p.Ser413Phe)	ASB18, GBX2-AS1 (S413F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 373441	NM_212556.4(ASB18):c.1286G>A (p.Arg429His)	ASB18, GBX2-AS1 (R429H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar