ClinVar Miner

List of variants reported as likely pathogenic for 3-M syndrome by Mendelics

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_014780.5(CUL7):c.2862+2T>G rs2150321832
NM_015311.3(OBSL1):c.1534+5G>C rs775172922

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