Related gene-specific medical variations for Gene (Select 9560) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2647686	NM_207007.4(CCL4L1):c.208G>A (p.Gly70Ser)	CCL4L1, CCL4L2 (G70S)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2647685	NM_207007.4(CCL4L1):c.192-6C>G	CCL4L1, CCL4L2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2647684	NM_207007.4(CCL4L1):c.192-69G>C	CCL4L1, CCL4L2	Single nucleotide variant (intron variant)	not provided	GLikely benign

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