List of variants in gene SHOC2 reported as benign for cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_007373.4(SHOC2):c.1161+42T>C	rs1980869	0.82744
NM_007373.4(SHOC2):c.*1503A>G	rs1327552	0.06997
NM_007373.4(SHOC2):c.*1487del	rs143768227	0.06116
NM_007373.4(SHOC2):c.457C>T (p.Leu153=)	rs34081996	0.01281
NM_007373.4(SHOC2):c.*773G>A	rs114628508	0.00719
NM_007373.4(SHOC2):c.1423-7C>T	rs180671383	0.00563
NM_007373.4(SHOC2):c.*697C>T	rs189140753	0.00453
NM_007373.4(SHOC2):c.1594A>G (p.Ser532Gly)	rs145463534	0.00423
NM_007373.4(SHOC2):c.-159T>C	rs72819758	0.00305
NM_007373.4(SHOC2):c.*164T>A	rs191293913	0.00283
NM_007373.4(SHOC2):c.*1775T>C	rs535776105	0.00157
NM_007373.4(SHOC2):c.*1483G>A	rs180979375	0.00128
NM_007373.4(SHOC2):c.*3T>C	rs143187497	0.00097
NM_007373.4(SHOC2):c.-179T>A	rs143180451	0.00080
NM_007373.4(SHOC2):c.704-16G>T	rs185614302	0.00033
NM_007373.4(SHOC2):c.*1323C>T	rs371721188	0.00021
NM_007373.4(SHOC2):c.841+12G>A	rs201258692	0.00019
NM_007373.4(SHOC2):c.*16C>A	rs753327392	0.00013
NM_007373.4(SHOC2):c.*1106A>C	rs118172559	0.00010
NM_007373.4(SHOC2):c.1161+9A>G	rs201795589	0.00008
NM_007373.4(SHOC2):c.1239G>T (p.Gln413His)	rs200215822	0.00006
NM_007373.4(SHOC2):c.610A>G (p.Ile204Val)	rs200015085	0.00006
NM_007373.4(SHOC2):c.*20C>T	rs371005619	0.00005
NM_007373.4(SHOC2):c.10A>C (p.Ser4Arg)	rs397517231	0.00004
NM_007373.4(SHOC2):c.*914G>A	rs189223963	0.00002
NM_007373.4(SHOC2):c.1541-7del	rs371544139
NM_007373.4(SHOC2):c.973-5del	rs730881016

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