List of variants in gene INSR reported as benign by Genetic Services Laboratory, University of Chicago

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000208.4(INSR):c.5C>G (p.Ala2Gly)	rs7508518	0.99996
NM_000208.4(INSR):c.653-7del	rs766817873	0.01724
NM_000208.4(INSR):c.653-9del	rs754360103	0.01255
NM_000208.4(INSR):c.1098T>C (p.Ser366=)	rs2229435	0.00988
NM_000208.4(INSR):c.909G>A (p.Gln303=)	rs9282757	0.00950
NM_000208.4(INSR):c.262T>C (p.Leu88=)	rs61736580	0.00797
NM_000208.4(INSR):c.2683-5C>T	rs41306363	0.00664
NM_000208.4(INSR):c.618C>T (p.Val206=)	rs56012021	0.00580
NM_000208.4(INSR):c.870C>T (p.His290=)	rs74483718	0.00416
NM_000208.4(INSR):c.653-23TC[11]	rs3835070
NM_000208.4(INSR):c.653-23TC[12]	rs3835070
NM_000208.4(INSR):c.653-23TC[14]	rs3835070
NM_000208.4(INSR):c.653-23TC[9]	rs3835070

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