ClinVar Miner

List of variants reported as uncertain significance for Bartter disease type 4B by Genomic Research Center, Shahid Beheshti University of Medical Sciences

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_004070.4(CLCNKA):c.55C>T (p.Gln19Ter) rs202069201 0.00006
NM_004070.4(CLCNKA):c.1613G>C (p.Arg538Pro) rs762119830
NM_004070.4(CLCNKA):c.17G>A (p.Gly6Glu) rs773206825

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