ClinVar Miner

List of variants in gene RAB18 reported as uncertain significance for Warburg micro syndrome

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP
NC_000010.11:g.27504220G>A
NM_001256410.1(RAB18):c.-144T>A rs780539442
NM_001256410.1(RAB18):c.-182G>A rs770568854
NM_001256410.1(RAB18):c.-79T>A rs886046964
NM_021252.5(RAB18):c.*1041A>G
NM_021252.5(RAB18):c.*1047T>G
NM_021252.5(RAB18):c.*1089C>A rs189434439
NM_021252.5(RAB18):c.*1110A>G
NM_021252.5(RAB18):c.*1136G>A rs753649409
NM_021252.5(RAB18):c.*1141T>C rs751708158
NM_021252.5(RAB18):c.*1452G>A
NM_021252.5(RAB18):c.*1502G>C rs767488036
NM_021252.5(RAB18):c.*150C>A
NM_021252.5(RAB18):c.*150C>T rs768390542
NM_021252.5(RAB18):c.*1589T>C
NM_021252.5(RAB18):c.*1680A>T rs886046972
NM_021252.5(RAB18):c.*1696T>A rs886046973
NM_021252.5(RAB18):c.*16A>G rs886046968
NM_021252.5(RAB18):c.*1779A>T
NM_021252.5(RAB18):c.*1800A>G
NM_021252.5(RAB18):c.*1842A>G
NM_021252.5(RAB18):c.*1845G>T rs186064414
NM_021252.5(RAB18):c.*1895G>C rs746613469
NM_021252.5(RAB18):c.*1943G>A rs560571679
NM_021252.5(RAB18):c.*2030G>T rs750141100
NM_021252.5(RAB18):c.*2085A>C
NM_021252.5(RAB18):c.*2327T>C
NM_021252.5(RAB18):c.*2420C>A rs770379811
NM_021252.5(RAB18):c.*2788C>T rs886046974
NM_021252.5(RAB18):c.*2862T>C rs767741672
NM_021252.5(RAB18):c.*2943A>G rs886046975
NM_021252.5(RAB18):c.*2985T>G
NM_021252.5(RAB18):c.*3046_*3047dup rs886046976
NM_021252.5(RAB18):c.*3166C>T rs886046977
NM_021252.5(RAB18):c.*3167G>A rs546186493
NM_021252.5(RAB18):c.*3193C>T rs886046978
NM_021252.5(RAB18):c.*3222C>T
NM_021252.5(RAB18):c.*3227A>G
NM_021252.5(RAB18):c.*325C>G rs886046970
NM_021252.5(RAB18):c.*3293del rs573606717
NM_021252.5(RAB18):c.*3330G>C
NM_021252.5(RAB18):c.*3543G>A
NM_021252.5(RAB18):c.*3559C>T rs117041769
NM_021252.5(RAB18):c.*3599dup rs779470678
NM_021252.5(RAB18):c.*3701_*3704GACT[1] rs759695566
NM_021252.5(RAB18):c.*3729G>C rs530960985
NM_021252.5(RAB18):c.*3766C>A
NM_021252.5(RAB18):c.*382C>T rs886046971
NM_021252.5(RAB18):c.*3832C>A
NM_021252.5(RAB18):c.*3906G>A
NM_021252.5(RAB18):c.*3927A>G rs886046981
NM_021252.5(RAB18):c.*4008C>T
NM_021252.5(RAB18):c.*402T>C rs555933024
NM_021252.5(RAB18):c.*4038A>T
NM_021252.5(RAB18):c.*4039A>C rs886046982
NM_021252.5(RAB18):c.*407G>T
NM_021252.5(RAB18):c.*4185G>A
NM_021252.5(RAB18):c.*419G>A
NM_021252.5(RAB18):c.*557G>A rs77758705
NM_021252.5(RAB18):c.*560C>T
NM_021252.5(RAB18):c.*62C>T rs886046969
NM_021252.5(RAB18):c.*635G>A
NM_021252.5(RAB18):c.*741A>G rs114899806
NM_021252.5(RAB18):c.*764A>G rs749045175
NM_021252.5(RAB18):c.*822T>C
NM_021252.5(RAB18):c.*890G>A rs539207601
NM_021252.5(RAB18):c.*8G>A
NM_021252.5(RAB18):c.*906A>G
NM_021252.5(RAB18):c.*946G>T
NM_021252.5(RAB18):c.*956A>C rs770434733
NM_021252.5(RAB18):c.*992C>A rs763254596
NM_021252.5(RAB18):c.*99C>T rs767920219
NM_021252.5(RAB18):c.-41A>G rs770276006
NM_021252.5(RAB18):c.270C>A (p.Val90=) rs750139202
NM_021252.5(RAB18):c.298G>C (p.Asp100His) rs748274360
NM_021252.5(RAB18):c.36C>A (p.Leu12=) rs61757825
NM_021252.5(RAB18):c.394G>T (p.Asp132Tyr) rs190213580
NM_021252.5(RAB18):c.422G>A (p.Arg141Gln)
NM_021252.5(RAB18):c.454G>A (p.Ala152Thr) rs886046967
NM_021252.5(RAB18):c.68+10A>G rs886046965

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