ClinVar Miner

List of variants reported as not provided for combined oxidative phosphorylation defect type 24 by GenomeConnect, ClinGen

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_024678.6(NARS2):c.595-6T>G rs774848576 0.00003
GRCh37/hg19 11q14.1(chr11:78189174-78189989)x1

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