Related gene-specific medical variations for Gene (Select 64768) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3110379	NM_022755.6(IPPK):c.17T>C (p.Met6Thr)	IPPK, LOC130002069 (M6T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110378	NM_022755.6(IPPK):c.1270G>A (p.Val424Ile)	CENPP, IPPK (V424I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2551416	NM_022755.6(IPPK):c.1444G>A (p.Glu482Lys)	CENPP, IPPK (E482K)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2516762	NM_022755.6(IPPK):c.1399C>T (p.Arg467Cys)	CENPP, IPPK (R467C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2512366	NM_022755.6(IPPK):c.1375G>A (p.Val459Ile)	CENPP, IPPK (V459I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2469651	NM_022755.6(IPPK):c.1459G>A (p.Val487Ile)	CENPP, IPPK (V487I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2394885	NM_022755.6(IPPK):c.1336G>A (p.Glu446Lys)	CENPP, IPPK (E446K)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2216299	NM_022755.6(IPPK):c.1466A>G (p.His489Arg)	CENPP, IPPK (H489R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

ClinVar