ClinVar Miner

Submissions for variant NM_003052.5(SLC34A1):c.*179G>A (rs141664220)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000297393 SCV000456689 likely benign Hypophosphatemic Nephrolithiasis/Osteoporosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000343493 SCV000484109 likely benign Hereditary Angioedema 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000402942 SCV000484110 likely benign Factor XII deficiency disease 2016-06-14 criteria provided, single submitter clinical testing

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