ClinVar Miner

List of variants studied for peroxisomal disease by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

Included ClinVar conditions (82):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_015294.6(TRIM37):c.2367C>G (p.Asp789Glu) rs143642427 0.00033
NM_015294.6(TRIM37):c.2047G>A (p.Ala683Thr)
NM_015294.6(TRIM37):c.2824A>C (p.Ser942Arg)
NM_015294.6(TRIM37):c.296A>G (p.His99Arg)

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