ClinVar Miner

Submissions for variant GRCh37/hg19 5q35.3(chr5:176812675-176813587)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV001536041 SCV001752736 pathogenic Hypophosphatemic nephrolithiasis/osteoporosis 1; Fanconi renotubular syndrome 2; Hypercalcemia, infantile, 2 no assertion criteria provided clinical testing

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