ClinVar Miner

Submissions for variant NM_001098484.3(SLC4A4):c.2937+22C>T

gnomAD frequency: 0.85968  dbSNP: rs1453474
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001680507 SCV001898169 benign not provided 2021-05-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810235 SCV002057630 benign Autosomal recessive proximal renal tubular acidosis 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001680507 SCV005297935 benign not provided criteria provided, single submitter not provided

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