"Illumina Laboratory Services, Illumina"[submitter] AND "CSRP3-AS1"[ge - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 137036	NM_003476.4(CSRP3):c.-74A>C	CSRP3-AS1, CSRP3	Single nucleotide variant	not specified +2 more	GConflicting classifications of pathogenicity
Select item 303955	NM_003476.4(CSRP3):c.-162_-161AG[6]	CSRP3, CSRP3-AS1	Microsatellite	Dilated Cardiomyopathy, Dominant +1 more	GUncertain significance
Select item 303956	NM_003476.4(CSRP3):c.-157G>A	CSRP3, CSRP3-AS1	Single nucleotide variant	Hypertrophic cardiomyopathy 12	GUncertain significance
Select item 303957	NM_003476.4(CSRP3):c.-158A>G	CSRP3, CSRP3-AS1	Single nucleotide variant	Hypertrophic cardiomyopathy 12	GUncertain significance
Select item 303958	NM_003476.4(CSRP3):c.-161delG	CSRP3, CSRP3-AS1	Deletion	Dilated Cardiomyopathy, Dominant +1 more	GUncertain significance
Select item 303959	NM_003476.4(CSRP3):c.-180delA	CSRP3, CSRP3-AS1	Deletion	Dilated Cardiomyopathy, Dominant +1 more	GUncertain significance
Select item 303960	NM_003476.4(CSRP3):c.-163A>G	CSRP3, CSRP3-AS1	Single nucleotide variant	Hypertrophic cardiomyopathy 12	GUncertain significance
Select item 303961	NM_003476.4(CSRP3):c.-181delC	CSRP3, CSRP3-AS1	Deletion	Dilated Cardiomyopathy, Dominant +1 more	GUncertain significance
Select item 303962	NM_003476.4(CSRP3):c.-182delT	CSRP3, CSRP3-AS1	Deletion	Dilated Cardiomyopathy, Dominant +1 more	GUncertain significance
Select item 303963	NM_003476.4(CSRP3):c.-195G>A	CSRP3-AS1, CSRP3	Single nucleotide variant	Hypertrophic cardiomyopathy 12 +1 more	GUncertain significance
Select item 877187	NM_003476.4(CSRP3):c.-211C>T	CSRP3, CSRP3-AS1	Single nucleotide variant	Hypertrophic cardiomyopathy 12	GUncertain significance
Select item 368949	NM_003476.4(CSRP3):c.-252G>A	CSRP3, CSRP3-AS1	Single nucleotide variant	Dilated Cardiomyopathy, Dominant +1 more	GLikely benign