ClinVar Miner

List of variants in gene ROBO2 reported as uncertain significance for Vesicoureteral reflux 2

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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_001128929.3(ROBO2):c.97G>T (p.Gly33Ter) rs747011633 0.01950
NM_001395656.1(ROBO2):c.2443C>T (p.Arg815Trp) rs188582283 0.00410
NM_001395656.1(ROBO2):c.*1950T>G rs543178648 0.00295
NM_001395656.1(ROBO2):c.*2104A>G rs757318528 0.00086
NM_001395656.1(ROBO2):c.*1915C>T rs886058888 0.00023
NM_001395656.1(ROBO2):c.*1890G>A rs540810243 0.00022
NM_001395656.1(ROBO2):c.*3276T>C rs886058892 0.00018
NM_001395656.1(ROBO2):c.*850A>G rs747242444 0.00017
NM_001395656.1(ROBO2):c.*2195C>T rs372439657 0.00014
NM_001395656.1(ROBO2):c.218C>G (p.Thr73Ser) rs141593508 0.00013
NM_001395656.1(ROBO2):c.3926G>A (p.Arg1309Gln) rs138700841 0.00011
NM_001395656.1(ROBO2):c.*913A>G rs775229600 0.00009
NM_001395656.1(ROBO2):c.-110C>G rs542668375 0.00007
NM_001395656.1(ROBO2):c.*1013C>T rs886058880 0.00006
NM_001395656.1(ROBO2):c.*3313T>C rs538973204 0.00006
NM_001395656.1(ROBO2):c.*2886A>C rs886058891 0.00004
NM_001395656.1(ROBO2):c.*2921C>T rs551478391 0.00004
NM_001395656.1(ROBO2):c.1930C>T (p.Arg644Cys) rs763833545 0.00004
NM_001395656.1(ROBO2):c.*2370C>T rs886058889 0.00003
NM_001395656.1(ROBO2):c.*3894A>G rs886058897 0.00003
NM_001395656.1(ROBO2):c.3785C>T (p.Thr1262Ile) rs772069288 0.00003
NM_001395656.1(ROBO2):c.*3594T>A rs922396647 0.00002
NM_001395656.1(ROBO2):c.-482C>T rs886058874 0.00002
NM_001395656.1(ROBO2):c.1275A>G (p.Leu425=) rs373043627 0.00002
NM_001395656.1(ROBO2):c.372G>A (p.Ala124=) rs763736763 0.00002
NM_001395656.1(ROBO2):c.*2679G>A rs2095429263 0.00001
NM_001395656.1(ROBO2):c.*3536G>A rs886058894 0.00001
NM_001395656.1(ROBO2):c.-166C>T rs886058875 0.00001
NM_001395656.1(ROBO2):c.-562A>G rs886058873 0.00001
NM_001395656.1(ROBO2):c.-571C>G rs886058872 0.00001
NM_001395656.1(ROBO2):c.1666G>A (p.Ala556Thr) rs1458146298 0.00001
NM_001395656.1(ROBO2):c.2578G>C (p.Val860Leu) rs201250546 0.00001
NM_001395656.1(ROBO2):c.2846T>C (p.Ile949Thr) rs267607014 0.00001
NM_001395656.1(ROBO2):c.3297A>G (p.Gln1099=) rs779204556 0.00001
NM_001395656.1(ROBO2):c.775A>G (p.Lys259Glu) rs1208378237 0.00001
NM_001395656.1(ROBO2):c.*1075T>C rs886058881
NM_001395656.1(ROBO2):c.*1435C>A rs886058882
NM_001395656.1(ROBO2):c.*1488T>G rs2095420720
NM_001395656.1(ROBO2):c.*1516G>A rs886058883
NM_001395656.1(ROBO2):c.*1579A>G rs886058884
NM_001395656.1(ROBO2):c.*166T>C rs886058878
NM_001395656.1(ROBO2):c.*178C>G rs999102374
NM_001395656.1(ROBO2):c.*1888C>T rs886058886
NM_001395656.1(ROBO2):c.*1894A>G rs886058887
NM_001395656.1(ROBO2):c.*2591G>T rs2095428608
NM_001395656.1(ROBO2):c.*3363T>G rs1300423583
NM_001395656.1(ROBO2):c.*3516T>C rs2095435052
NM_001395656.1(ROBO2):c.*3707G>A rs2095436372
NM_001395656.1(ROBO2):c.*3804T>C rs2095437062
NM_001395656.1(ROBO2):c.*3809A>C rs886058896
NM_001395656.1(ROBO2):c.*947C>T rs550745516
NM_001395656.1(ROBO2):c.*972T>C rs886058879
NM_001395656.1(ROBO2):c.*985C>T rs114687906
NM_001395656.1(ROBO2):c.1244-1G>A rs1268364860
NM_001395656.1(ROBO2):c.1277A>G (p.Gln426Arg) rs1402671241
NM_001395656.1(ROBO2):c.1312A>G (p.Thr438Ala)
NM_001395656.1(ROBO2):c.1434G>A (p.Gln478=) rs1316651009
NM_001395656.1(ROBO2):c.1659C>G (p.Thr553=) rs879541755
NM_001395656.1(ROBO2):c.1670G>A (p.Ser557Asn) rs2093385370
NM_001395656.1(ROBO2):c.1845T>C (p.Asp615=) rs757943652
NM_001395656.1(ROBO2):c.3148+2T>C rs868180675
NM_001395656.1(ROBO2):c.335C>T (p.Ala112Val) rs780623744
NM_001395656.1(ROBO2):c.3379G>A (p.Glu1127Lys) rs1371853103
NM_001395656.1(ROBO2):c.339G>T (p.Arg113Ser) rs768750709
NM_001395656.1(ROBO2):c.371C>T (p.Ala124Val) rs762759644
NM_001395656.1(ROBO2):c.4262C>G (p.Pro1421Arg) rs900326063
NM_001395656.1(ROBO2):c.4349G>A (p.Arg1450His) rs771581041
NM_001395656.1(ROBO2):c.467C>T (p.Pro156Leu) rs2084155191
NM_001395656.1(ROBO2):c.558A>G (p.Gly186=) rs886058876
NM_001395656.1(ROBO2):c.628G>A (p.Gly210Arg) rs2084647233

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