ClinVar Miner

List of variants reported as benign for Rabson-Mendenhall syndrome

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ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_000208.4(INSR):c.5C>G (p.Ala2Gly) rs7508518 0.99996
NM_000208.4(INSR):c.*104A>G rs1051690 0.83181
NM_000208.4(INSR):c.*2779G>A rs3745551 0.67433
NM_000208.4(INSR):c.1483+31T>C rs2860178 0.52842
NM_000208.4(INSR):c.*1494G>A rs3745550 0.27864
NM_000208.4(INSR):c.1610+28A>C rs2860177 0.24043
NM_000208.4(INSR):c.*784C>G rs1051651 0.22772
NM_000208.4(INSR):c.*4474C>T rs1052371 0.22677
NM_000208.3(INSR):c.*4802C>T rs12150997 0.22638
NM_000208.4(INSR):c.1861+27C>T rs3815902 0.21056
NM_000208.4(INSR):c.3255C>T (p.His1085=) rs1799817 0.20288
NM_000208.4(INSR):c.1932A>C (p.Pro644=) rs2245655 0.12535
NM_000208.4(INSR):c.1862-4A>G rs2245649 0.12510
NM_000208.4(INSR):c.1918C>T (p.Leu640=) rs2963 0.12510
NM_000208.4(INSR):c.783C>T (p.Asp261=) rs891087 0.11869
NM_000208.4(INSR):c.*2854G>T rs1864193 0.10584
NM_000208.4(INSR):c.*4422G>T rs12642 0.10462
NM_000208.4(INSR):c.*2010G>A rs55972112 0.10448
NM_000208.4(INSR):c.2595C>T (p.Asn865=) rs2229431 0.08453
NM_000208.4(INSR):c.2007C>T (p.Phe669=) rs2962 0.08356
NM_000208.4(INSR):c.*4195T>C rs1366601 0.06149
NM_000208.4(INSR):c.*4186T>C rs1366600 0.06049
NM_000208.4(INSR):c.3033C>T (p.Tyr1011=) rs1799815 0.04745
NM_000208.4(INSR):c.*3029T>C rs72988602 0.04550
NM_000208.4(INSR):c.*3623A>G rs77859571 0.04400
NM_000208.4(INSR):c.*1974_*1975del rs148930499 0.02551
NM_000208.4(INSR):c.*224C>T rs2860171 0.02007
NM_000208.4(INSR):c.2643C>T (p.Ile881=) rs2229432 0.01903
NM_000208.4(INSR):c.2542+3A>G rs13306451 0.01900
NM_000208.4(INSR):c.2448G>A (p.Thr816=) rs2229434 0.01850
NM_000208.4(INSR):c.*1432C>T rs111557734 0.01814
NM_000208.4(INSR):c.*2793C>A rs9282760 0.01708
NM_000208.4(INSR):c.3795-5C>T rs78312382 0.01607
NM_000208.4(INSR):c.*3592A>G rs75499056 0.01497
NM_000208.3(INSR):c.*4794T>C rs10415841 0.01406
NM_000208.4(INSR):c.*4218G>C rs10416396 0.01362
NM_000208.4(INSR):c.2370G>A (p.Thr790=) rs16994210 0.01346
NM_000208.4(INSR):c.*2340A>G rs78987925 0.01226
NM_000208.4(INSR):c.*4602C>T rs10413914 0.01216
NM_000208.4(INSR):c.*3857C>T rs114405975 0.01204
NM_000208.4(INSR):c.*2519G>A rs114982195 0.01193
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.909G>A (p.Gln303=) rs9282757 0.00950
NM_000208.4(INSR):c.*3463A>G rs115358150 0.00928
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.*2502A>G rs149795309 0.00665
NM_000208.4(INSR):c.*1089A>G rs116422284 0.00664
NM_000208.4(INSR):c.2683-5C>T rs41306363 0.00664
NM_000208.4(INSR):c.*3786G>C rs115012090 0.00642
NM_000208.4(INSR):c.618C>T (p.Val206=) rs56012021 0.00580
NM_000208.4(INSR):c.1123+13G>T rs72549236 0.00526
NM_000208.4(INSR):c.3034G>A (p.Val1012Met) rs1799816 0.00500
NM_000208.4(INSR):c.870C>T (p.His290=) rs74483718 0.00416
NM_000208.4(INSR):c.*4270G>A rs74433419 0.00386
NM_000208.4(INSR):c.*3541C>T rs116953519 0.00271
NM_000208.4(INSR):c.2682+9C>G rs41398545 0.00145
NM_000208.4(INSR):c.2388G>C (p.Arg796Ser) rs78433961 0.00036
NM_000208.4(INSR):c.*1416del rs3833238
NM_000208.4(INSR):c.*288del rs35434645
NM_000208.4(INSR):c.*930dup rs34045095
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.2526G>C (p.Ala842=) rs2229430
NM_000208.4(INSR):c.653-23TC[11] rs3835070

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