ClinVar Miner

List of variants studied for autosomal recessive polycystic kidney disease by Department of Molecular and Human Genetics, Baylor College of Medicine

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 6p12.3-12.2(chr6:51695623-52371918)
NM_138694.4(PKHD1):c.10452dup (p.Leu3485fs) rs771623148

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