Related gene-specific medical variations for Gene (Select 54798) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685132	GRCh37/hg19 4q31.3(chr4:155065505-155159162)x1	DCHS2	Copy number loss	not provided	GUncertain significance
Select item 2685131	GRCh37/hg19 4q31.3(chr4:154957240-155205078)x1	DCHS2	Copy number loss	not provided	GUncertain significance
Select item 2501772	NM_001358235.2(DCHS2):c.4019-835_4019-834insA	DCHS2 (M1343fs)	Insertion (frameshift variant +1 more)	Multiple congenital anomalies	GUncertain significance
Select item 685981	GRCh37/hg19 4q31.3(chr4:154769596-155177347)x3	DCHS2	Copy number gain	not provided	GUncertain significance
Select item 161708	NM_001358235.2(DCHS2):c.4375G>A (p.Gly1459Arg)	DCHS2 (G1459R)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 91995	NM_001358235.2(DCHS2):c.2053-7021A>G	DCHS2	Single nucleotide variant (intron variant)	not provided	GUncertain significance

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