Related gene-specific medical variations for Gene (Select 3621) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3286006	NM_198219.3(ING1):c.136+1247T>C	ING1, LOC130010137 (M30T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3286005	NM_198219.3(ING1):c.136+1310G>C	ING1, LOC130010137 (R51P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286002	NM_198219.3(ING1):c.136+1234G>C	ING1, LOC130010137 (A26P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618560	NM_198219.3(ING1):c.136+1267C>A	ING1, LOC130010137 (L37I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558261	NM_198219.3(ING1):c.136+1349C>G	ING1, LOC130010137 (P64R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328563	NM_198219.3(ING1):c.136+1304G>A	ING1, LOC130010137 (G49D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279610	NM_198219.3(ING1):c.136+1388C>T	ING1, LOC130010137 (S77F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar