List of variants in gene SGCD reported as likely benign for Limb-girdle muscular dystrophy, recessive

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 52

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.*4092A>G	rs56389540	0.09897
NM_000337.6(SGCD):c.*5114C>T	rs3913482	0.08930
NM_000337.6(SGCD):c.*3650G>T	rs72803044	0.08674
NM_000337.6(SGCD):c.*7814C>T	rs56233900	0.08591
NM_000337.6(SGCD):c.*2365T>C	rs72803042	0.08564
NM_000337.6(SGCD):c.*5990T>A	rs72803047	0.08555
NM_000337.6(SGCD):c.*2712T>C	rs56293630	0.08538
NM_000337.6(SGCD):c.*1373A>G	rs72803041	0.08347
NM_000337.6(SGCD):c.*360A>G	rs72803040	0.08345
NM_000337.6(SGCD):c.*3687A>G	rs72803046	0.08194
NM_000337.6(SGCD):c.*3962G>A	rs56182215	0.08020
NM_000337.6(SGCD):c.*6665G>A	rs61633788	0.07733
NM_000337.6(SGCD):c.*4166T>C	rs55653598	0.06787
NM_000337.6(SGCD):c.*3413G>C	rs72803043	0.06601
NM_000337.6(SGCD):c.*7300C>A	rs72803048	0.06455
NC_000005.10:g.156326973A>T	rs7725121	0.06375
NM_000337.6(SGCD):c.290G>A (p.Arg97Gln)	rs45559835	0.04192
NM_000337.6(SGCD):c.*4498G>A	rs73304958	0.03775
NM_000337.6(SGCD):c.*363C>T	rs6886827	0.03518
NM_000337.6(SGCD):c.*7596A>G	rs80115276	0.02244
NM_000337.6(SGCD):c.*4895G>A	rs115905727	0.01677
NM_000337.6(SGCD):c.*6400C>T	rs10065295	0.01419
NM_000337.6(SGCD):c.*3898C>T	rs74717343	0.01308
NM_000337.6(SGCD):c.*4818G>A	rs76466586	0.01301
NM_000337.6(SGCD):c.*2236T>C	rs183838407	0.00964
NM_000337.6(SGCD):c.*7816G>A	rs78589560	0.00921
NC_000005.10:g.156327097A>G	rs77808502	0.00918
NM_000337.6(SGCD):c.*822C>T	rs78615220	0.00735
NM_000337.6(SGCD):c.*2697T>C	rs146249602	0.00722
NM_000337.6(SGCD):c.507G>A (p.Ala169=)	rs10071079	0.00635
NM_000337.6(SGCD):c.294+8T>C	rs11748588	0.00606
NM_000337.6(SGCD):c.*5877C>A	rs117879283	0.00430
NM_000337.6(SGCD):c.*7866G>A	rs115728448	0.00408
NM_000337.6(SGCD):c.*4638C>A	rs187538595	0.00363
NM_000337.6(SGCD):c.*3868C>A	rs181847929	0.00353
NM_000337.6(SGCD):c.*6917C>T	rs549743616	0.00346
NM_000337.6(SGCD):c.*3292A>G	rs148505840	0.00334
NM_000337.6(SGCD):c.*6683T>C	rs73304961	0.00283
NM_000337.6(SGCD):c.1846_1847dup	rs527436848	0.00273
NM_000337.6(SGCD):c.*5348T>C	rs149021597	0.00222
NM_000337.6(SGCD):c.*1112G>A	rs566338494	0.00199
NM_000337.6(SGCD):c.*5663A>G	rs151214419	0.00180
NM_000337.6(SGCD):c.*6430G>A	rs185162959	0.00120
NM_000337.6(SGCD):c.213G>A (p.Arg71=)	rs74846539	0.00115
NM_000337.6(SGCD):c.*5226G>A	rs552358256	0.00051
NM_000337.6(SGCD):c.510G>A (p.Glu170=)	rs368838376	0.00029
NM_000337.6(SGCD):c.*150G>T	rs147791150	0.00023
NM_000337.6(SGCD):c.848A>G (p.Gln283Arg)	rs397516338	0.00020
NM_000337.6(SGCD):c.-404G>A	rs192662989	0.00016
NM_000337.6(SGCD):c.15G>C (p.Glu5Asp)	rs549319429	0.00004
NM_000337.6(SGCD):c.*2814G>T	rs142023087
NM_000337.6(SGCD):c.*5723del	rs147634470

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