List of variants reported as benign for Left ventricular noncompaction 1

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_001386795.1(DTNA):c.1743+14G>A	rs1617318	0.36560
NM_001386795.1(DTNA):c.1903+17T>C	rs541157	0.15990
NM_001386795.1(DTNA):c.1903+8G>A	rs111817603	0.01438
NM_001386795.1(DTNA):c.1821G>A (p.Ala607=)	rs9959365	0.00984
NM_001386795.1(DTNA):c.537G>T (p.Thr179=)	rs11877640	0.00956
NM_001386795.1(DTNA):c.933C>T (p.Ser311=)	rs114170541	0.00902
NM_001386795.1(DTNA):c.2162+14G>A	rs76713874	0.00820
NM_001386795.1(DTNA):c.1438C>A (p.Pro480Thr)	rs77320474	0.00558
NM_001386795.1(DTNA):c.210G>A (p.Leu70=)	rs117571555	0.00440
NM_001386795.1(DTNA):c.1993+7T>C	rs138590000	0.00403
NM_001386795.1(DTNA):c.1435-19T>C	rs141620769	0.00328
NM_001386795.1(DTNA):c.243A>G (p.Leu81=)	rs146923532	0.00285
NM_001386795.1(DTNA):c.999C>T (p.Ile333=)	rs61737438	0.00242
NM_001386795.1(DTNA):c.1176-8T>C	rs41274310	0.00232
NM_001386795.1(DTNA):c.604-14G>T	rs397517447	0.00126
NM_001386795.1(DTNA):c.1000G>A (p.Val334Met)	rs148123045	0.00120
NM_001386795.1(DTNA):c.2178A>C (p.Ala726=)	rs145486636	0.00063
NM_001386795.1(DTNA):c.92G>A (p.Arg31Gln)	rs202046233	0.00063
NM_001386795.1(DTNA):c.231C>T (p.Asn77=)	rs147759402	0.00047
NM_001386795.1(DTNA):c.1002-2330A>G	rs369005625	0.00008
NM_001386795.1(DTNA):c.1454G>C (p.Ser485Thr)	rs190619495	0.00007
NM_001386795.1(DTNA):c.1875G>A (p.Gly625=)	rs542483546	0.00004
NM_001386795.1(DTNA):c.93A>G (p.Arg31=)	rs778817036	0.00004
NM_001386795.1(DTNA):c.2295+15G>A	rs756945985	0.00002
NM_001386795.1(DTNA):c.1532+18T>C	rs115712655
NM_001386795.1(DTNA):c.1744-10G>A	rs192561043
NM_001386795.1(DTNA):c.1744-10G>T	rs192561043
NM_001386795.1(DTNA):c.710-5dup	rs2518051890

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