Related gene-specific medical variations for Gene (Select 6348) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139750	NM_002983.3(CCL3):c.158C>T (p.Thr53Met)	CCL3, CCL3-AS1 (T53M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139749	NM_002983.3(CCL3):c.118C>T (p.Arg40Trp)	CCL3, CCL3-AS1 (R40W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591827	NM_002983.3(CCL3):c.203G>A (p.Arg68Gln)	CCL3, CCL3-AS1 (R68Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393178	NM_002983.3(CCL3):c.182G>T (p.Gly61Val)	CCL3, CCL3-AS1 (G61V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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