List of variants in gene SGCD studied for Cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.507G>A (p.Ala169=)	rs10071079	0.00680
NM_000337.6(SGCD):c.294+8T>C	rs11748588	0.00640
NM_000337.6(SGCD):c.*2A>C	rs200757725	0.00241
NM_000337.6(SGCD):c.213G>A (p.Arg71=)	rs74846539	0.00115
NM_000337.6(SGCD):c.144G>C (p.Val48=)	rs372152495	0.00106
NM_000337.6(SGCD):c.510G>A (p.Glu170=)	rs368838376	0.00029
NM_000337.6(SGCD):c.92G>A (p.Arg31Gln)	rs200476861	0.00016
NM_000337.6(SGCD):c.402T>C (p.Ala134=)	rs190935424	0.00007
NM_000337.6(SGCD):c.15G>C (p.Glu5Asp)	rs549319429	0.00004
NM_000337.6(SGCD):c.767C>T (p.Thr256Met)	rs578056399	0.00003
NM_000337.6(SGCD):c.105G>C (p.Leu35=)	rs193922392
NM_000337.6(SGCD):c.274A>C (p.Lys92Gln)	rs1159364901

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