ClinVar Miner

List of variants in gene RET reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.3040-311A>G rs2742239 0.84034
NM_020975.6(RET):c.2137-324A>G rs741968 0.83977
NM_020975.6(RET):c.*1506G>A rs2742241 0.83094
NM_020975.6(RET):c.2136+271T>C rs1864399 0.79711
NM_020975.6(RET):c.2392+302G>A rs2075910 0.79521
NM_020975.6(RET):c.1263+272A>G rs1864403 0.79336
NM_020975.6(RET):c.1064-89A>T rs1864404 0.79203
NM_020975.6(RET):c.868-75T>C rs2742243 0.76941
NM_020975.6(RET):c.2731-290A>G rs2565202 0.57732
NM_020975.6(RET):c.2137-167T>C rs2256550 0.57070
NM_020975.6(RET):c.73+172A>C rs12246856 0.42677
NM_020975.6(RET):c.74-126G>T rs2565206 0.37985
NM_020975.6(RET):c.73+53G>A rs12267460 0.37428
NM_020975.6(RET):c.73+171_73+172del rs1425791427 0.36953
NM_020975.6(RET):c.337+137G>T rs2505530 0.30933
NM_020975.6(RET):c.867+223A>T rs1864406 0.28874
NM_020975.6(RET):c.*1116T>C rs2435355 0.22170
NM_020975.6(RET):c.625+118A>G rs2472739 0.20776
NM_020975.6(RET):c.135= (p.Ala45=) rs1800858 0.20726
NM_020975.6(RET):c.337+9G>A rs2435351 0.20641
NM_020975.6(RET):c.2608-24G>A rs2472737 0.20380
NM_020975.6(RET):c.2284+47C>T rs760466 0.18873
NM_020975.6(RET):c.2730+257C>T rs2435353 0.17317
NM_020975.6(RET):c.2940-197C>T rs3026781 0.17069
NM_020975.6(RET):c.2608-147C>T rs11238441 0.17019
NM_020975.6(RET):c.2071G>A (p.Gly691Ser) rs1799939 0.16640
NM_020975.6(RET):c.1759+111G>C rs3026757 0.05904
NM_020975.6(RET):c.2730+322C>T rs3026769 0.05154
NM_020975.6(RET):c.2730+229T>C rs3026768 0.04385
NM_020975.6(RET):c.2731-227C>G rs3026771 0.04259
NM_020975.6(RET):c.*1969T>C rs3026785 0.04255
NM_020975.6(RET):c.2508C>T (p.Ser836=) rs1800862 0.03791
NM_020975.6(RET):c.1522+308C>G rs3026748 0.03146
NM_020975.6(RET):c.2608-124G>A rs111306965 0.02876
NM_020975.6(RET):c.2940-252G>A rs11238443 0.02839
NM_020975.6(RET):c.1649-187C>T rs7358114 0.01897
NM_020975.6(RET):c.2137-253C>T rs74135468 0.01804
NM_020975.6(RET):c.2944C>T (p.Arg982Cys) rs17158558 0.01567
NM_020975.6(RET):c.868-18G>A rs57098408 0.01028
NM_020975.6(RET):c.338-106G>A rs73252046 0.01016
NM_020975.6(RET):c.2285-85G>A rs3026766 0.01001
NM_020975.6(RET):c.375C>A (p.Val125=) rs1800859 0.00877
NM_020975.6(RET):c.1648+188G>A rs3026753 0.00771
NM_020975.6(RET):c.2801+72G>A rs3026773 0.00574
NM_020975.6(RET):c.2801+54A>T rs3026772 0.00391
NM_020975.6(RET):c.1760-140C>G rs3026758 0.00376
NM_020975.6(RET):c.1063+47G>A rs372177579 0.00315
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe) rs77724903 0.00178
NM_020975.6(RET):c.1465G>A (p.Asp489Asn) rs9282834 0.00068
NM_020975.6(RET):c.833C>A (p.Thr278Asn) rs35118262 0.00056
NM_020975.6(RET):c.341G>A (p.Arg114His) rs76397662 0.00029
NM_020975.6(RET):c.1759+242G>A rs78601594
NM_020975.6(RET):c.1760-57G>T rs2132824724
NM_020975.6(RET):c.2136+182G>A rs1864400
NM_020975.6(RET):c.2393-94C>A rs111264957
NM_020975.6(RET):c.3187+198T>A rs2075913
NM_020975.6(RET):c.626-72_626-71del rs144431581
NM_020975.6(RET):c.73+173_73+174insCGGGCGGCG rs1483784179
NM_020975.6(RET):c.74-57del rs57003029
NM_020975.6(RET):c.74-57dup rs57003029

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