ClinVar Miner

List of variants in gene ROBO2 studied 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: 118
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HGVS dbSNP
NM_001128929.3(ROBO2):c.*1013C>T rs886058880
NM_001128929.3(ROBO2):c.*1040T>G rs539305333
NM_001128929.3(ROBO2):c.*1052G>A rs535435438
NM_001128929.3(ROBO2):c.*1061C>T rs186113368
NM_001128929.3(ROBO2):c.*1075T>C rs886058881
NM_001128929.3(ROBO2):c.*1114G>A rs11127602
NM_001128929.3(ROBO2):c.*1216C>T rs1031377
NM_001128929.3(ROBO2):c.*121G>A rs139789773
NM_001128929.3(ROBO2):c.*1245T>A rs559415425
NM_001128929.3(ROBO2):c.*1290G>T rs568949141
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.*1619dup rs530776423
NM_001128929.3(ROBO2):c.*166T>C rs886058878
NM_001128929.3(ROBO2):c.*1739A>G rs114621892
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.*1950T>G rs543178648
NM_001128929.3(ROBO2):c.*1958C>T rs147850774
NM_001128929.3(ROBO2):c.*1959G>C rs183377310
NM_001128929.3(ROBO2):c.*2104A>G rs757318528
NM_001128929.3(ROBO2):c.*2195C>T rs372439657
NM_001128929.3(ROBO2):c.*2196G>A rs117129934
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.*2668T>G rs554356923
NM_001128929.3(ROBO2):c.*2675C>G rs183103458
NM_001128929.3(ROBO2):c.*2737G>A rs1163748
NM_001128929.3(ROBO2):c.*2789G>A rs187992106
NM_001128929.3(ROBO2):c.*2819T>G rs191290792
NM_001128929.3(ROBO2):c.*2865T>C rs116956967
NM_001128929.3(ROBO2):c.*2886A>C rs886058891
NM_001128929.3(ROBO2):c.*2964A>T rs1163749
NM_001128929.3(ROBO2):c.*3001A>G rs114795420
NM_001128929.3(ROBO2):c.*3151A>G rs115587257
NM_001128929.3(ROBO2):c.*3183G>A rs73845747
NM_001128929.3(ROBO2):c.*3236G>A rs1163750
NM_001128929.3(ROBO2):c.*3276T>C rs886058892
NM_001128929.3(ROBO2):c.*3288del rs566529890
NM_001128929.3(ROBO2):c.*3313T>C rs538973204
NM_001128929.3(ROBO2):c.*3536G>A rs886058894
NM_001128929.3(ROBO2):c.*3608dup rs548297436
NM_001128929.3(ROBO2):c.*3618T>C rs192514111
NM_001128929.3(ROBO2):c.*3725T>C rs149616306
NM_001128929.3(ROBO2):c.*3809A>C rs886058896
NM_001128929.3(ROBO2):c.*3873C>T rs538922713
NM_001128929.3(ROBO2):c.*3894A>G rs886058897
NM_001128929.3(ROBO2):c.*3923C>T rs10865561
NM_001128929.3(ROBO2):c.*486A>T rs181305605
NM_001128929.3(ROBO2):c.*610T>C rs186391329
NM_001128929.3(ROBO2):c.*699G>T rs564667813
NM_001128929.3(ROBO2):c.*947C>T rs550745516
NM_001128929.3(ROBO2):c.*972T>C rs886058879
NM_001128929.3(ROBO2):c.*985C>A rs114687906
NM_001128929.3(ROBO2):c.*985C>T rs114687906
NM_001128929.3(ROBO2):c.1038A>G (p.Thr346=) rs146036715
NM_001128929.3(ROBO2):c.110-14G>T rs61731268
NM_001128929.3(ROBO2):c.110-57338C>G rs542668375
NM_001128929.3(ROBO2):c.110-57394C>T rs886058875
NM_001128929.3(ROBO2):c.110-57466T>G rs3923744
NM_001128929.3(ROBO2):c.110-57632G>C rs79942150
NM_001128929.3(ROBO2):c.110-57687G>A rs542280581
NM_001128929.3(ROBO2):c.110-57710C>T rs886058874
NM_001128929.3(ROBO2):c.110-57770T>C rs3923745
NM_001128929.3(ROBO2):c.110-57790A>G rs886058873
NM_001128929.3(ROBO2):c.110-57799C>G rs886058872
NM_001128929.3(ROBO2):c.1108-10G>A rs115485646
NM_001128929.3(ROBO2):c.1205C>T (p.Ala402Val) rs199705591
NM_001128929.3(ROBO2):c.1332G>T (p.Thr444=) rs191732065
NM_001128929.3(ROBO2):c.1357C>T (p.Leu453=) rs773786584
NM_001128929.3(ROBO2):c.142C>A (p.Arg48=) rs6788280
NM_001128929.3(ROBO2):c.1592A>T (p.Asn531Ile) rs80051448
NM_001128929.3(ROBO2):c.1742G>C (p.Ser581Thr) rs761048204
NM_001128929.3(ROBO2):c.1841T>C (p.Ile614Thr) rs185792666
NM_001128929.3(ROBO2):c.1881T>C (p.Asp627=) rs757943652
NM_001128929.3(ROBO2):c.1897+15T>C rs770007839
NM_001128929.3(ROBO2):c.1897+8C>G rs144780438
NM_001128929.3(ROBO2):c.1992T>C (p.Thr664=) rs61731263
NM_001128929.3(ROBO2):c.19C>A (p.Arg7Ser) rs12171318
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.2066G>A (p.Arg689His) rs376737394
NM_001128929.3(ROBO2):c.2122C>T (p.Pro708Ser) rs187796411
NM_001128929.3(ROBO2):c.2377-12C>A rs115128094
NM_001128929.3(ROBO2):c.2442C>T (p.Ser814=) rs200412132
NM_001128929.3(ROBO2):c.2479C>T (p.Arg827Trp) rs188582283
NM_001128929.3(ROBO2):c.2480G>A (p.Arg827Gln) rs199675194
NM_001128929.3(ROBO2):c.2774+9C>T rs573265362
NM_001128929.3(ROBO2):c.2882T>C (p.Ile961Thr) rs267607014
NM_001128929.3(ROBO2):c.3009T>C (p.Ser1003=) rs200717956
NM_001128929.3(ROBO2):c.3105A>G (p.Gln1035=) rs544425952
NM_001128929.3(ROBO2):c.3184+2T>C rs868180675
NM_001128929.3(ROBO2):c.3185-14G>A rs188399309
NM_001128929.3(ROBO2):c.3456C>T (p.Gly1152=) rs143561771
NM_001128929.3(ROBO2):c.3520C>T (p.Arg1174Trp) rs747971442
NM_001128929.3(ROBO2):c.3602+13del rs78824327
NM_001128929.3(ROBO2):c.3711C>T (p.Ala1237=) rs774727452
NM_001128929.3(ROBO2):c.3754G>A (p.Ala1252Thr) rs267607015
NM_001128929.3(ROBO2):c.3801T>C (p.Ser1267=) rs201292837
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.3905G>T (p.Arg1302Leu) rs200131009
NM_001128929.3(ROBO2):c.3924G>A (p.Lys1308=) rs200933374
NM_001128929.3(ROBO2):c.4086C>T (p.Thr1362=) rs201527229
NM_001128929.3(ROBO2):c.4104C>T (p.Gly1368=) rs184958084
NM_001128929.3(ROBO2):c.4112G>A (p.Arg1371His) rs771581041
NM_001128929.3(ROBO2):c.4183+5G>C rs373371736
NM_001128929.3(ROBO2):c.510C>T (p.Cys170=) rs200353960
NM_001128929.3(ROBO2):c.519C>T (p.Pro173=) rs201406456
NM_001128929.3(ROBO2):c.595-3C>T rs113680429
NM_001128929.3(ROBO2):c.606A>G (p.Gly202=) rs886058876
NM_001128929.3(ROBO2):c.73G>A (p.Val25Met) rs78834776
NM_001128929.3(ROBO2):c.855-7T>A rs200430970
NM_001128929.3(ROBO2):c.978C>T (p.Val326=) rs370244031
NM_001128929.3(ROBO2):c.97G>T (p.Gly33Ter) rs747011633

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