List of variants in gene SGCD reported as benign for autosomal recessive limb-girdle muscular dystrophy type 2F

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.*6717G>A	rs1827368	0.90216
NM_000337.6(SGCD):c.84T>C (p.Tyr28=)	rs1801193	0.39558
NM_000337.6(SGCD):c.*3772dup	rs397841758	0.20069
NM_000337.6(SGCD):c.*5863C>T	rs11953631	0.15411
NM_000337.6(SGCD):c.*4092A>G	rs56389540	0.09897
NM_000337.6(SGCD):c.*3650G>T	rs72803044	0.08674
NM_000337.6(SGCD):c.290G>A (p.Arg97Gln)	rs45559835	0.04292
NM_000337.6(SGCD):c.*7596A>G	rs80115276	0.02244
NM_000337.6(SGCD):c.700-19T>C	rs80086857	0.02231
NM_000337.6(SGCD):c.295-40T>A	rs74571343	0.01950
NM_000337.6(SGCD):c.*822C>T	rs78615220	0.00715
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.144G>C (p.Val48=)	rs372152495	0.00106
NM_000337.6(SGCD):c.699+18C>G	rs180898690	0.00019
NM_000337.6(SGCD):c.3+20G>A	rs187786098	0.00013
NM_000337.6(SGCD):c.3+11C>T	rs374790317	0.00010
NM_000337.6(SGCD):c.15G>C (p.Glu5Asp)	rs549319429	0.00004
NM_000337.6(SGCD):c.3+14G>A	rs538229806	0.00003
NM_000337.5(SGCD):c.-626_-616del	rs149976574
NM_000337.6(SGCD):c.-94C>G	rs13170573
NM_000337.6(SGCD):c.105G>C (p.Leu35=)	rs193922392
NM_000337.6(SGCD):c.226G>T (p.Gly76Cys)	rs376659221
NM_000337.6(SGCD):c.503-16del	rs1561835980
NM_000337.6(SGCD):c.516A>G (p.Thr172=)	rs753952200
NM_000337.6(SGCD):c.699+13_699+15del	rs397517924

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