ClinVar Miner

List of variants in gene CYP4F22 studied for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_173483.4(CYP4F22):c.*421dup rs886054265
NM_173483.4(CYP4F22):c.939+15_939+16del rs537649124
NM_173483.4(CYP4F22):c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA rs886054264

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