ClinVar Miner

Submissions for variant NM_000186.4(CFH):c.350+15C>T

dbSNP: rs190197472
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002168318 SCV002422731 benign not provided 2022-12-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494324 SCV002800399 likely benign Basal laminar drusen; Factor H deficiency; Hemolytic uremic syndrome, atypical, susceptibility to, 1; Age related macular degeneration 4 2021-10-17 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003447036 SCV004172486 benign Hemolytic uremic syndrome, atypical, susceptibility to, 1 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003447039 SCV004172487 benign Age related macular degeneration 4 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003447038 SCV004172488 benign Basal laminar drusen 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003447037 SCV004172489 benign Factor H deficiency 2023-04-11 criteria provided, single submitter clinical testing

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