ClinVar Miner

List of variants in gene CERS1, GDF1 studied for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
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HGVS dbSNP
NM_001492.6(GDF1):c.-1049C>T rs561672108
NM_001492.6(GDF1):c.-1065G>A rs1038592004
NM_001492.6(GDF1):c.-1066C>T rs374895377
NM_001492.6(GDF1):c.-1073C>A
NM_001492.6(GDF1):c.-1079T>C
NM_001492.6(GDF1):c.-1101C>G
NM_001492.6(GDF1):c.-1142C>A rs1330389032
NM_001492.6(GDF1):c.-1145C>T rs760185006
NM_001492.6(GDF1):c.-1159T>A rs918114133
NM_001492.6(GDF1):c.-1286C>T rs868136098
NM_001492.6(GDF1):c.-1300C>G rs1568309719
NM_001492.6(GDF1):c.-1307C>A rs1041161328
NM_001492.6(GDF1):c.-1318_-1316CGG[4]
NM_001492.6(GDF1):c.-305C>G rs774114834
NM_001492.6(GDF1):c.-312-2A>G rs771873576
NM_001492.6(GDF1):c.-334G>T
NM_001492.6(GDF1):c.-417C>T rs377364343
NM_001492.6(GDF1):c.-422-3C>A rs1464119106
NM_001492.6(GDF1):c.-425C>T rs373928623
NM_001492.6(GDF1):c.-466C>T rs559340743
NM_001492.6(GDF1):c.-472T>C rs1568297877
NM_001492.6(GDF1):c.-487C>G
NM_001492.6(GDF1):c.-489C>T rs781327266
NM_001492.6(GDF1):c.-536G>A rs200539084
NM_001492.6(GDF1):c.-581G>A
NM_001492.6(GDF1):c.-615T>A rs902153714
NM_001492.6(GDF1):c.-638G>A
NM_001492.6(GDF1):c.-733+9A>G rs200695801
NM_001492.6(GDF1):c.-741C>T rs779941388
NM_001492.6(GDF1):c.-748C>T
NM_001492.6(GDF1):c.-764C>G rs772627907
NM_001492.6(GDF1):c.-766C>T
NM_001492.6(GDF1):c.-773G>T rs374308521
NM_001492.6(GDF1):c.-774C>G rs200024180
NM_001492.6(GDF1):c.-830G>A
NM_001492.6(GDF1):c.-831C>T rs45601540
NM_001492.6(GDF1):c.-846T>C rs1426719277
NM_001492.6(GDF1):c.-873C>T rs201106410
NM_001492.6(GDF1):c.-886G>A rs201005099
NM_001492.6(GDF1):c.-894A>G rs200107216
NM_001492.6(GDF1):c.-904C>T
NM_001492.6(GDF1):c.-925C>T rs1555707050
NM_001492.6(GDF1):c.925T>C (p.Ser309Pro) rs864622513

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