ClinVar Miner

List of variants in gene NFE2L2 reported as likely pathogenic 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: 8
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HGVS dbSNP
NM_001313903.1(NFE2L2):c.93+142G>C rs1057519922
NM_001313903.1(NFE2L2):c.93+143A>T rs1057519923
NM_001313903.1(NFE2L2):c.93+144G>T rs1057519924
NM_001313904.1(NFE2L2):c.-144A>G rs1057519921
NM_001313904.1(NFE2L2):c.-145G>A rs1057519920
NM_001313904.1(NFE2L2):c.-145G>C rs1057519920
NM_001313904.1(NFE2L2):c.-145G>T rs1057519920
NM_006164.5(NFE2L2):c.235G>A (p.Glu79Lys) rs1057519922

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