ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.2963T>A (p.Met988Lys)

gnomAD frequency: 0.00001  dbSNP: rs748479566
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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
Eurofins Ntd Llc (ga) RCV000733335 SCV000861386 uncertain significance not provided 2018-05-23 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002485929 SCV002785333 uncertain significance Dubin-Johnson syndrome 2021-08-25 criteria provided, single submitter clinical testing

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