ClinVar Miner

List of variants in gene combination CERT1, POLK reported as uncertain significance by Institute of Human Genetics, University of Goettingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 5q13.3(chr5:74744212-74806334)x1
NM_001130105.1(CERT1):c.67G>A (p.Val23Ile)

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