ClinVar Miner

Submissions for variant NM_002438.4(MRC1):c.1186G>A (p.Gly396Ser)

gnomAD frequency: 0.31451  dbSNP: rs606231248
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000054833 SCV000083078 risk factor Susceptibility to leprosy and multibacillary leprosy 2010-03-01 no assertion criteria provided literature only
Centro Dermatológico Federico Lleras Acosta, Hospital Universitario Centro Dermatológico Federico Lleras Acosta RCV002291554 SCV002583885 uncertain risk allele Leprosy, susceptibility to, 1 2022-06-10 no assertion criteria provided case-control

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