ClinVar Miner

Submissions for variant NM_019888.3(MC3R):c.437T>A (p.Ile146Asn)

gnomAD frequency: 0.00001  dbSNP: rs74315393
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000022657 SCV000043946 risk factor OBESITY (BMIQ9), SUSCEPTIBILITY TO 2004-08-01 no assertion criteria provided literature only

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