ClinVar Miner

List of variants in gene VANGL1 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_138959.3(VANGL1):c.*1183del rs3841008 0.25316
NM_138959.3(VANGL1):c.*3544C>T rs74117023 0.01618
NM_138959.3(VANGL1):c.*3336G>A rs61732170 0.01470
NM_138959.3(VANGL1):c.-239G>A rs563855412 0.00806
NM_138959.3(VANGL1):c.*1652C>T rs146512242 0.00738
NM_138959.3(VANGL1):c.*5444C>G rs142497673 0.00486
NM_138959.3(VANGL1):c.435T>C (p.Cys145=) rs34768472 0.00443
NM_138959.3(VANGL1):c.*3653C>T rs146435279 0.00442
NM_138959.3(VANGL1):c.*2865A>G rs114921471 0.00424
NM_138959.3(VANGL1):c.345C>T (p.Val115=) rs79828493 0.00413
NM_138959.3(VANGL1):c.*2336A>G rs148944333 0.00362
NM_138959.3(VANGL1):c.330C>T (p.Tyr110=) rs41275546 0.00358
NM_138959.3(VANGL1):c.*1772A>G rs114033235 0.00199
NM_138959.3(VANGL1):c.323A>G (p.Lys108Arg) rs141673853 0.00154
NM_138959.3(VANGL1):c.*383C>G rs75277108 0.00153
NM_138959.3(VANGL1):c.*5466G>A rs192325588 0.00135
NM_138959.3(VANGL1):c.*2187T>C rs146730302 0.00061
NM_138959.3(VANGL1):c.73G>A (p.Glu25Lys) rs61734296 0.00048
NM_138959.3(VANGL1):c.*47G>T rs190792695 0.00039
NM_138959.3(VANGL1):c.1172G>T (p.Arg391Met) rs140485834 0.00022
NM_138959.3(VANGL1):c.231G>A (p.Thr77=) rs186509771 0.00014
NM_138959.3(VANGL1):c.868T>C (p.Tyr290His) rs145309218 0.00014
NM_138959.3(VANGL1):c.*1545A>G rs117337677 0.00012
NM_138959.3(VANGL1):c.1127A>G (p.Gln376Arg) rs200389969 0.00009
NM_138959.3(VANGL1):c.98C>T (p.Ser33Leu) rs78535164 0.00009
NM_138959.3(VANGL1):c.1299C>T (p.Asn433=) rs145137292 0.00006
NM_138959.3(VANGL1):c.812+9C>T rs370321176 0.00006
NM_138959.3(VANGL1):c.*707C>T rs562969850 0.00005
NM_138959.3(VANGL1):c.51G>A (p.Ser17=) rs575493003 0.00004
NM_138959.3(VANGL1):c.1023C>T (p.Asn341=) rs543050989 0.00003
NM_138959.3(VANGL1):c.*2344A>C rs531884184 0.00001
NM_138959.3(VANGL1):c.114C>T (p.Asp38=) rs201840785 0.00001
NM_138959.3(VANGL1):c.572T>C (p.Val191Ala) rs781010619 0.00001
NM_138959.3(VANGL1):c.*3762CAAA[2] rs144395099
NM_138959.3(VANGL1):c.*4089del rs138659832
NM_138959.3(VANGL1):c.*4788C>G rs148437823
NM_138959.3(VANGL1):c.*5008T>A rs117347999

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