ClinVar Miner

Submissions for variant GRCh38/hg38 Yq11.222(chrY:17251756-19149935)x2

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 8 RCV000135753 SCV000175715 benign See cases 2010-10-20 no assertion criteria provided clinical testing
ISCA site 1 RCV000135753 SCV000175716 conflicting data from submitters See cases 2011-01-05 no assertion criteria provided clinical testing Uncertain significance(1), Likely benign (1)

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