Variants in gene SGCG with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_000231.3(SGCG):c.-6T>C	rs141771521	0.00749
NM_000231.3(SGCG):c.*185G>A	rs115918628	0.00447
NM_000231.3(SGCG):c.539A>T (p.Glu180Val)	rs114160429	0.00101
NM_000231.3(SGCG):c.832G>A (p.Gly278Ser)	rs147820869	0.00049
NM_000231.3(SGCG):c.102C>T (p.Arg34=)	rs140810408	0.00011
NM_000231.3(SGCG):c.497G>A (p.Arg166Gln)	rs776289036	0.00009
NM_000231.3(SGCG):c.506-7T>G	rs774582375	0.00009
NM_000231.3(SGCG):c.414A>G (p.Gln138=)	rs770596449	0.00005
NM_000231.3(SGCG):c.1-8C>T	rs745599370	0.00001
NM_000231.3(SGCG):c.267A>G (p.Pro89=)	rs149595403	0.00001
NM_000231.3(SGCG):c.*136T>A	rs3751372
NM_000231.3(SGCG):c.507G>T (p.Gly169=)	rs199905729

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