ClinVar Miner

List of variants in gene NFE2L2 reported as likely pathogenic for cervix disorder

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_006164.5(NFE2L2):c.235G>A (p.Glu79Lys) rs1057519922
NM_006164.5(NFE2L2):c.235G>C (p.Glu79Gln) rs1057519922
NM_006164.5(NFE2L2):c.236A>T (p.Glu79Val) rs1057519923
NM_006164.5(NFE2L2):c.237G>T (p.Glu79Asp) rs1057519924
NM_006164.5(NFE2L2):c.85G>A (p.Asp29Asn) rs1057519920
NM_006164.5(NFE2L2):c.85G>C (p.Asp29His) rs1057519920
NM_006164.5(NFE2L2):c.85G>T (p.Asp29Tyr) rs1057519920
NM_006164.5(NFE2L2):c.86A>G (p.Asp29Gly) rs1057519921

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