List of variants in gene INSR reported by Personalized Diabetes Medicine Program, University of Maryland School of Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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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.2971C>A (p.Leu991Ile)	rs150114699	0.00307
NM_000208.4(INSR):c.2838C>G (p.Asp946Glu)	rs146588336	0.00145
NM_000208.4(INSR):c.2575C>T (p.His859Tyr)	rs149536206	0.00123
NM_000208.4(INSR):c.2243C>T (p.Ser748Leu)	rs143523271	0.00116
NM_000208.4(INSR):c.41T>C (p.Leu14Pro)	rs745857330	0.00047
NM_000208.4(INSR):c.2388G>C (p.Arg796Ser)	rs78433961	0.00036
NM_000208.4(INSR):c.224A>G (p.Asp75Gly)	rs142910337	0.00029
NM_000208.4(INSR):c.2564G>A (p.Gly855Asp)	rs201667363	0.00001
NM_000208.4(INSR):c.1459A>C (p.Lys487Gln)	rs121913136
NM_000208.4(INSR):c.1741C>T (p.Arg581Trp)	rs1555743340

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