ClinVar Miner

List of variants reported as benign for Warburg micro syndrome

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 69
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HGVS dbSNP
NM_001256410.1(RAB18):c.-83C>A rs115326586
NM_012233.3(RAB3GAP1):c.*1077T>C rs16831395
NM_012233.3(RAB3GAP1):c.*1208del rs200869351
NM_012233.3(RAB3GAP1):c.*135C>G rs10170125
NM_012233.3(RAB3GAP1):c.*1378T>C rs59746814
NM_012233.3(RAB3GAP1):c.*171G>A rs11558413
NM_012233.3(RAB3GAP1):c.*1826G>C
NM_012233.3(RAB3GAP1):c.*261dup rs143703110
NM_012233.3(RAB3GAP1):c.*404C>T rs149483456
NM_012233.3(RAB3GAP1):c.*992G>A
NM_012233.3(RAB3GAP1):c.*995T>C rs116237324
NM_012233.3(RAB3GAP1):c.1041A>G (p.Arg347=) rs77972211
NM_012233.3(RAB3GAP1):c.1793A>G (p.Asn598Ser) rs10445686
NM_012233.3(RAB3GAP1):c.1992G>A (p.Ser664=) rs7595725
NM_012233.3(RAB3GAP1):c.2265T>C (p.Phe755=) rs17261772
NM_012233.3(RAB3GAP1):c.2463C>T (p.Phe821=) rs61748693
NM_012233.3(RAB3GAP1):c.2800C>G (p.Pro934Ala) rs77535003
NM_012233.3(RAB3GAP1):c.357A>G (p.Val119=) rs73959261
NM_012233.3(RAB3GAP1):c.669G>T (p.Leu223Phe) rs76927619
NM_012233.3(RAB3GAP1):c.913A>G (p.Ile305Val) rs116775947
NM_012414.4(RAB3GAP2):c.*1130A>G rs548918189
NM_012414.4(RAB3GAP2):c.*1504G>T rs41303053
NM_012414.4(RAB3GAP2):c.*2043G>A rs367962640
NM_012414.4(RAB3GAP2):c.*2920_*2922CTT[1] rs3217443
NM_012414.4(RAB3GAP2):c.*404T>C rs1059140
NM_012414.4(RAB3GAP2):c.*925C>T rs185747953
NM_012414.4(RAB3GAP2):c.1709A>G (p.Asn570Ser) rs143286302
NM_012414.4(RAB3GAP2):c.1779+7G>A rs111345353
NM_012414.4(RAB3GAP2):c.2008C>G (p.Leu670Val) rs201613456
NM_012414.4(RAB3GAP2):c.2088A>G (p.Thr696=) rs2577126
NM_012414.4(RAB3GAP2):c.2304G>A (p.Leu768=) rs140146408
NM_012414.4(RAB3GAP2):c.2587A>G (p.Thr863Ala) rs12045447
NM_012414.4(RAB3GAP2):c.3275G>C (p.Ser1092Thr) rs2289189
NM_012414.4(RAB3GAP2):c.3495G>A (p.Leu1165=) rs11547779
NM_012414.4(RAB3GAP2):c.3924G>C (p.Thr1308=) rs73098539
NM_012414.4(RAB3GAP2):c.3966A>G (p.Lys1322=) rs150226729
NM_012414.4(RAB3GAP2):c.3991C>A (p.Leu1331Ile) rs149842844
NM_012414.4(RAB3GAP2):c.39C>T (p.Asp13=) rs145667920
NM_012414.4(RAB3GAP2):c.713-12T>C rs76473498
NM_012414.4(RAB3GAP2):c.774A>G (p.Leu258=) rs576411922
NM_012414.4(RAB3GAP2):c.812-6del rs35396665
NM_021252.5(RAB18):c.*1412C>T rs10508723
NM_021252.5(RAB18):c.*1488A>C rs148630305
NM_021252.5(RAB18):c.*1542T>C rs10508724
NM_021252.5(RAB18):c.*2375A>G rs2477317
NM_021252.5(RAB18):c.*2449A>G rs12260532
NM_021252.5(RAB18):c.*2476G>A rs12267298
NM_021252.5(RAB18):c.*2529G>A rs145293804
NM_021252.5(RAB18):c.*2744C>T rs12254670
NM_021252.5(RAB18):c.*278A>T rs41282848
NM_021252.5(RAB18):c.*3129C>T rs78270485
NM_021252.5(RAB18):c.*3453G>A rs11015861
NM_021252.5(RAB18):c.*3476A>G rs11597728
NM_021252.5(RAB18):c.*3484T>C rs11598268
NM_021252.5(RAB18):c.*3521C>T
NM_021252.5(RAB18):c.*3584C>T rs11015862
NM_021252.5(RAB18):c.*3696T>A rs10829269
NM_021252.5(RAB18):c.*3803_*3804insT rs3832657
NM_021252.5(RAB18):c.*387C>A rs12248740
NM_021252.5(RAB18):c.*3939A>T rs1047915
NM_021252.5(RAB18):c.*3967T>C
NM_021252.5(RAB18):c.*4131A>G
NM_021252.5(RAB18):c.*448G>A
NM_021252.5(RAB18):c.*504A>G rs12571836
NM_021252.5(RAB18):c.*757G>T rs76051289
NM_021252.5(RAB18):c.*758A>T rs10508722
NM_021252.5(RAB18):c.-20C>T rs74127323
NM_021252.5(RAB18):c.260-7dup rs142609338
NM_021252.5(RAB18):c.592G>A (p.Ala198Thr) rs11015859

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