ClinVar Miner

List of variants in gene ROBO2 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_001128929.3(ROBO2):c.*1013C>T rs886058880
NM_001128929.3(ROBO2):c.*1075T>C rs886058881
NM_001128929.3(ROBO2):c.*1245T>A rs559415425
NM_001128929.3(ROBO2):c.*1435C>A rs886058882
NM_001128929.3(ROBO2):c.*1516G>A rs886058883
NM_001128929.3(ROBO2):c.*1579A>G rs886058884
NM_001128929.3(ROBO2):c.*166T>C rs886058878
NM_001128929.3(ROBO2):c.*1888C>T rs886058886
NM_001128929.3(ROBO2):c.*1894A>G rs886058887
NM_001128929.3(ROBO2):c.*1915C>T rs886058888
NM_001128929.3(ROBO2):c.*2104A>G rs757318528
NM_001128929.3(ROBO2):c.*2195C>T rs372439657
NM_001128929.3(ROBO2):c.*2355T>A rs766386654
NM_001128929.3(ROBO2):c.*2370C>T rs886058889
NM_001128929.3(ROBO2):c.*2570C>A rs886058890
NM_001128929.3(ROBO2):c.*2886A>C rs886058891
NM_001128929.3(ROBO2):c.*3276T>C rs886058892
NM_001128929.3(ROBO2):c.*3313T>C rs538973204
NM_001128929.3(ROBO2):c.*3536G>A rs886058894
NM_001128929.3(ROBO2):c.*3809A>C rs886058896
NM_001128929.3(ROBO2):c.*3894A>G rs886058897
NM_001128929.3(ROBO2):c.*972T>C rs886058879
NM_001128929.3(ROBO2):c.*985C>T rs114687906
NM_001128929.3(ROBO2):c.110-57394C>T rs886058875
NM_001128929.3(ROBO2):c.110-57710C>T rs886058874
NM_001128929.3(ROBO2):c.110-57790A>G rs886058873
NM_001128929.3(ROBO2):c.110-57799C>G rs886058872
NM_001128929.3(ROBO2):c.1205C>T (p.Ala402Val) rs199705591
NM_001128929.3(ROBO2):c.1357C>T (p.Leu453=) rs773786584
NM_001128929.3(ROBO2):c.1742G>C (p.Ser581Thr) rs761048204
NM_001128929.3(ROBO2):c.1881T>C (p.Asp627=) rs757943652
NM_001128929.3(ROBO2):c.1897+15T>C rs770007839
NM_001128929.3(ROBO2):c.2020G>A (p.Val674Ile) rs372550683
NM_001128929.3(ROBO2):c.2055A>C (p.Arg685=) rs886058877
NM_001128929.3(ROBO2):c.2479C>T (p.Arg827Trp) rs188582283
NM_001128929.3(ROBO2):c.3105A>G (p.Gln1035=) rs544425952
NM_001128929.3(ROBO2):c.3184+2T>C rs868180675
NM_001128929.3(ROBO2):c.3520C>T (p.Arg1174Trp) rs747971442
NM_001128929.3(ROBO2):c.3711C>T (p.Ala1237=) rs774727452
NM_001128929.3(ROBO2):c.3821C>T (p.Thr1274Ile) rs772069288
NM_001128929.3(ROBO2):c.383C>T (p.Ala128Val) rs780623744
NM_001128929.3(ROBO2):c.4112G>A (p.Arg1371His) rs771581041
NM_001128929.3(ROBO2):c.4183+5G>C rs373371736
NM_001128929.3(ROBO2):c.606A>G (p.Gly202=) rs886058876
NM_001128929.3(ROBO2):c.97G>T (p.Gly33Ter) rs747011633

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