ClinVar Miner

List of variants in gene INSR reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_000208.3(INSR):c.653-5_653-4del rs3835070
NM_000208.4(INSR):c.1483+31T>C rs2860178
NM_000208.4(INSR):c.1610+23C>T rs9676400
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.2231+20C>A rs6413502
NM_000208.4(INSR):c.2842+33G>A rs35169098
NM_000208.4(INSR):c.3033C>T (p.Tyr1011=) rs1799815
NM_000208.4(INSR):c.3034G>A (p.Val1012Met) rs1799816
NM_000208.4(INSR):c.3255C>T (p.His1085=) rs1799817
NM_000208.4(INSR):c.3259-31C>T rs148813626
NM_000208.4(INSR):c.5C>G (p.Ala2Gly) rs7508518
NM_000208.4(INSR):c.653-23TC[11] rs3835070
NM_000208.4(INSR):c.653-9_653-7delinsC rs1568470641
NM_000208.4(INSR):c.783C>T (p.Asp261=) rs891087
NM_000208.4(INSR):c.870C>T (p.His290=) rs74483718

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