ClinVar Miner

List of variants reported as uncertain significance for Bartter disease type 4A by Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine

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
NM_057176.3(BSND):c.35T>C (p.Ile12Thr) rs121908144 0.00002
NM_057176.3(BSND):c.52C>G (p.Leu18Val) rs754403589

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