ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
NM_000208.4(INSR):c.1123+21G>A rs13306458
NM_000208.4(INSR):c.1610+23C>T rs9676400
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.2231+20C>A rs6413502
NM_000208.4(INSR):c.2267+17C>T rs41509747
NM_000208.4(INSR):c.2595C>T (p.Asn865=) rs2229431
NM_000208.4(INSR):c.262T>C (p.Leu88=) rs61736580
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.653-23TC[9] 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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.