Related gene-specific medical variations for Gene (Select 6366) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139725	NM_002989.4(CCL21):c.362G>T (p.Gly121Val)	CCL21, PHF24 (G121V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139724	NM_002989.4(CCL21):c.284C>A (p.Ser95Tyr)	CCL21, PHF24 (S95Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402630	NM_002989.4(CCL21):c.277A>G (p.Thr93Ala)	CCL21, PHF24 (T93A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398484	NM_002989.4(CCL21):c.380G>A (p.Arg127Gln)	CCL21, PHF24 (R127Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2334921	NM_002989.4(CCL21):c.197C>A (p.Pro66His)	CCL21, PHF24 (P66H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279117	NM_002989.4(CCL21):c.124G>T (p.Ala42Ser)	CCL21, PHF24 (A42S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221802	NM_002989.4(CCL21):c.376G>A (p.Glu126Lys)	CCL21, PHF24 (E126K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 792124	NM_002989.4(CCL21):c.288A>G (p.Pro96=)	CCL21, PHF24	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar