Related gene-specific medical variations for Gene (Select 387837) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2530760	NM_001129998.3(CLEC12B):c.449A>G (p.Tyr150Cys)	CLEC12B, LOC102724020 (Y47C +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2398143	NM_001129998.3(CLEC12B):c.695A>G (p.Glu232Gly)	CLEC12B, LOC102724020 (E129G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2395433	NM_001129998.3(CLEC12B):c.649T>C (p.Trp217Arg)	CLEC12B, LOC102724020 (W217R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2311290	NM_001129998.3(CLEC12B):c.511G>A (p.Asp171Asn)	CLEC12B, LOC102724020 (D171N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2294846	NM_001129998.3(CLEC12B):c.712G>C (p.Gly238Arg)	CLEC12B, LOC102724020 (G135R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2270865	NM_001129998.3(CLEC12B):c.794A>T (p.Lys265Met)	CLEC12B, LOC102724020 (K236M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235236	NM_001129998.3(CLEC12B):c.521A>C (p.Asp174Ala)	CLEC12B, LOC102724020 (D174A +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2229910	NM_001129998.3(CLEC12B):c.419G>T (p.Cys140Phe)	CLEC12B, LOC102724020 (C37F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance