Variants in gene INSR with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000208.4(INSR):c.3034G>A (p.Val1012Met)	rs1799816	0.00500
NM_000208.4(INSR):c.2355G>A (p.Ser785=)	rs148137322	0.00285
NM_000208.4(INSR):c.2736G>A (p.Arg912=)	rs147125937	0.00134
NM_000208.4(INSR):c.190T>C (p.Leu64=)	rs144836032	0.00092
NM_000208.4(INSR):c.2970G>A (p.Pro990=)	rs41304772	0.00085
NM_000208.4(INSR):c.1550A>G (p.Glu517Gly)	rs147671523	0.00058
NM_000208.4(INSR):c.41T>C (p.Leu14Pro)	rs745857330	0.00047
NM_000208.4(INSR):c.4133G>A (p.Arg1378Gln)	rs52826008

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