"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "CRYAB"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3026280	NM_001289808.2(CRYAB):c.495G>C (p.Glu165Asp)	CRYAB (E165D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 41926	NM_001289808.2(CRYAB):c.460G>A (p.Gly154Ser)	CRYAB (G154S +1 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +10 more	GConflicting classifications of pathogenicity
Select item 217346	NM_001289808.2(CRYAB):c.320G>T (p.Arg107Leu)	CRYAB (R107L +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1II +1 more	GConflicting classifications of pathogenicity
Select item 44232	NM_001289808.2(CRYAB):c.152C>T (p.Pro51Leu)	CRYAB (P51L)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1II +8 more	GConflicting classifications of pathogenicity
Select item 1150664	NM_001289808.2(CRYAB):c.84C>T (p.Phe28=)	CRYAB	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 546688	NM_001289808.2(CRYAB):c.19C>T (p.His7Tyr)	CRYAB (H7Y)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

ClinVar