List of variants in gene INSR reported as likely benign by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000208.4(INSR):c.2643C>T (p.Ile881=)	rs2229432	0.01903
NM_000208.4(INSR):c.1989G>A (p.Ala663=)	rs36081066	0.01045
NM_000208.4(INSR):c.1098T>C (p.Ser366=)	rs2229435	0.00988
NM_000208.4(INSR):c.2718T>C (p.Ala906=)	rs2229433	0.00891
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.2193G>A (p.Thr731=)	rs6413501	0.00350
NM_000208.4(INSR):c.1080C>T (p.Cys360=)	rs56066516	0.00183
NM_000208.4(INSR):c.2736G>A (p.Arg912=)	rs147125937	0.00134
NM_000208.4(INSR):c.687C>T (p.Thr229=)	rs150568177	0.00111
NM_000208.4(INSR):c.190T>C (p.Leu64=)	rs144836032	0.00092
NM_000208.4(INSR):c.2793G>A (p.Ala931=)	rs111502197	0.00088
NM_000208.4(INSR):c.2295C>T (p.Gly765=)	rs142654992	0.00058
NM_000208.4(INSR):c.225C>T (p.Asp75=)	rs41352749	0.00011
NM_000208.4(INSR):c.2829C>T (p.Tyr943=)	rs376766937	0.00008
NM_000208.4(INSR):c.624A>G (p.Arg208=)	rs759705666	0.00001

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