ClinVar Miner

List of variants reported as pathogenic for 2q24 microdeletion syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 2q24.2-31.1(chr2:160347642-174075851)x1
GRCh37/hg19 2q24.2-31.3(chr2:163078055-182119617)x1

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