ClinVar Miner

Submissions for variant NM_000183.3(HADHB):c.210-1G>C

dbSNP: rs200777054
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000239550 SCV000297841 uncertain significance not provided 2016-08-16 no assertion criteria provided literature only
Inherited Neuropathy Consortium RCV000789677 SCV000929052 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only

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