ClinVar Miner

Submissions for variant NM_003002.4(SDHD):c.*803A>G (rs17113461)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000037726 SCV000061388 benign not specified 2012-12-21 criteria provided, single submitter clinical testing *803A>G in 3'UTR of SDHD: This variant has been identified in 9.2% of chromosome s from a broad, though clinically and racially unspecified population by the 100 0 Genomes project (dbSNP rs17113461). Although this region can contain elements that regulate mRNA, there is no obvious predicted effect of this variant. *80 3A>G in 3'UTR of SDHD(rs17113461; allele frequency = 9.2%)
Illumina Clinical Services Laboratory,Illumina RCV000399051 SCV000367364 benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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