ClinVar Miner

List of variants reported as benign for Neural tube defect

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_138959.3(VANGL1):c.*505A>G rs6700610 0.67885
NM_020335.3(VANGL2):c.1137A>G (p.Lys379=) rs12086448 0.58424
NM_138959.3(VANGL1):c.*4478C>T rs17034226 0.41876
NM_138959.3(VANGL1):c.*2351T>G rs12121158 0.41872
NM_138959.3(VANGL1):c.*5751A>G rs10801933 0.41406
NM_138959.3(VANGL1):c.*5368G>A rs10494179 0.39762
NM_138959.3(VANGL1):c.*5995A>T rs4595366 0.39755
NM_138959.3(VANGL1):c.*5841A>T rs4548441 0.39752
NM_138959.3(VANGL1):c.*3496T>A rs4839472 0.31126
NM_138959.3(VANGL1):c.*416G>A rs3811011 0.25321
NM_138959.3(VANGL1):c.*1277C>T rs3204955 0.25318
NM_138959.3(VANGL1):c.*3023G>T rs10923204 0.24904
NM_138959.3(VANGL1):c.*6026G>A rs6428677 0.24227
NM_138959.3(VANGL1):c.*6199A>T rs3811007 0.22923
NM_138959.3(VANGL1):c.*83T>A rs3811013 0.17099
NM_138959.3(VANGL1):c.*6212C>T rs3811006 0.16816
NM_138959.3(VANGL1):c.*4504C>T rs17034228 0.16812
NM_138959.3(VANGL1):c.*5266C>T rs17034230 0.16811
NM_138959.3(VANGL1):c.346G>A (p.Ala116Thr) rs4839469 0.12684
NM_138959.3(VANGL1):c.-224C>A rs191609592 0.10807
NM_138959.3(VANGL1):c.*6721A>G rs17034249 0.10611
NM_138959.3(VANGL1):c.*2581G>A rs3811008 0.10587
NM_138959.3(VANGL1):c.*3417C>T rs76160883 0.06248
NM_138959.3(VANGL1):c.*2489C>T rs41299571 0.06245
NM_138959.3(VANGL1):c.*6321T>G rs77318780 0.06169
NM_138959.3(VANGL1):c.*300C>T rs41310108 0.05806
NM_138959.3(VANGL1):c.*217C>T rs41299565 0.05793
NM_138959.3(VANGL1):c.*694C>A rs41312690 0.05722
NM_138959.3(VANGL1):c.*2043C>T rs74117021 0.02749
NM_138959.3(VANGL1):c.1040A>C (p.Glu347Ala) rs34059106 0.01695
NM_138959.3(VANGL1):c.*1627A>G rs149888685 0.00606
NM_138959.3(VANGL1):c.285C>T (p.Ile95=) rs140451005 0.00060
NM_138959.3(VANGL1):c.248C>T (p.Ser83Leu) rs146695372 0.00010
NM_138959.3(VANGL1):c.518G>A (p.Arg173His) rs148341022 0.00003
NM_020335.3(VANGL2):c.403C>T (p.Arg135Trp)
NM_138959.3(VANGL1):c.*1749G>T rs3811010
NM_138959.3(VANGL1):c.*313A>G rs3811012
NM_138959.3(VANGL1):c.*5633T>G rs4348723
NM_138959.3(VANGL1):c.-226G>C rs116216703

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