ClinVar Miner

Submissions for variant NM_000231.3(SGCG):c.607A>G (p.Met203Val)

dbSNP: rs1883002488
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Natera, Inc. RCV001277473 SCV001464427 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2C 2020-04-19 no assertion criteria provided clinical testing

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