ClinVar Miner

List of variants studied for amelogenesis imperfecta type 2 by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_004917.5(KLK4):c.224+2T>C rs201555681 0.00001
NM_182758.4(WDR72):c.1348+1G>T rs1431736022
NM_182758.4(WDR72):c.858-1G>C rs2017517553

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