Related gene-specific medical variations for Gene (Select 126805691) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3078187	NM_001281956.2(CSMD2):c.6389G>C (p.Gly2130Ala)	CSMD2, LOC126805691 (G2130A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078186	NM_001281956.2(CSMD2):c.6347A>G (p.Tyr2116Cys)	CSMD2, LOC126805691 (Y2118C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078183	NM_001281956.2(CSMD2):c.6344-435G>A	CSMD2, LOC126805691 (V2103I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3078182	NM_001281956.2(CSMD2):c.6344-463G>C	CSMD2, LOC126805691 (E2093D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512306	NM_001281956.2(CSMD2):c.6344-429G>A	CSMD2, LOC126805691 (A2105T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466467	NM_001281956.2(CSMD2):c.6344-473A>G	CSMD2, LOC126805691 (D2090G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403983	NM_001281956.2(CSMD2):c.6344-422A>G	CSMD2, LOC126805691 (Y2107C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358111	NM_001281956.2(CSMD2):c.6344-423T>C	CSMD2, LOC126805691 (Y2107H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343804	NM_001281956.2(CSMD2):c.6344-453A>G	CSMD2, LOC126805691 (T2097A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334881	NM_001281956.2(CSMD2):c.6446C>T (p.Pro2149Leu)	CSMD2, LOC126805691 (P2149L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance