ClinVar Miner

List of variants in gene DMD reported as likely pathogenic by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
GRCh37/hg19 Xp21.1(chrX:31815807-31875058)x0
NM_004006.2(DMD):c.7660+1G>C rs1556852444
NM_004006.2(DMD):c.79dup (p.Ala27fs) rs1057519180

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