ClinVar Miner

Submissions for variant NM_005430.4(WNT1):c.859dup (p.His287fs)

dbSNP: rs387907353
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000043491 SCV000067314 pathogenic Osteogenesis imperfecta type 15 2013-04-04 no assertion criteria provided literature only
OMIM RCV000043492 SCV000067315 risk factor OSTEOPOROSIS, EARLY-ONSET, SUSCEPTIBILITY TO 2013-04-04 no assertion criteria provided literature only

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