ClinVar Miner

List of variants in gene INSR reported as benign for none provided

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Gene type:
ClinVar version:
Total variants: 13
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NM_000208.4(INSR):c.1483+31T>C rs2860178
NM_000208.4(INSR):c.1610+28A>C rs2860177
NM_000208.4(INSR):c.1638C>T (p.Asp546=) rs2229429
NM_000208.4(INSR):c.1650G>A (p.Ala550=) rs2059806
NM_000208.4(INSR):c.1861+27C>T rs3815902
NM_000208.4(INSR):c.1862-20A>G rs2245648
NM_000208.4(INSR):c.1862-4A>G rs2245649
NM_000208.4(INSR):c.1918C>T (p.Leu640=) rs2963
NM_000208.4(INSR):c.1932A>C (p.Pro644=) rs2245655
NM_000208.4(INSR):c.2007C>T (p.Phe669=) rs2962
NM_000208.4(INSR):c.3255C>T (p.His1085=) rs1799817
NM_000208.4(INSR):c.5C>G (p.Ala2Gly) rs7508518
NM_000208.4(INSR):c.783C>T (p.Asp261=) rs891087

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