ClinVar Miner

List of variants in gene combination LRRC38, PDPN reported as uncertain significance for aortic disease

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
GRCh37/hg19 1p36.21(chr1:13801823-14012604)

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