ClinVar Miner

List of variants reported as likely benign for Non-syndromic X-linked intellectual disability by Illumina Laboratory Services, Illumina

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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_024921.4(POF1B):c.*1173C>A rs7062790 0.01314
NM_024921.4(POF1B):c.*1808A>G rs56307558 0.00517
NM_001330574.2(ZNF711):c.*1411G>A rs779890560 0.00296
NM_001330574.2(ZNF711):c.*1260G>A rs73234669 0.00178
NM_004840.3(ARHGEF6):c.685G>A (p.Val229Ile) rs75329154 0.00146
NM_004840.3(ARHGEF6):c.*131_*134del rs775186031 0.00080
NM_001330574.2(ZNF711):c.-473GGC[9] rs758475553
NM_004840.3(ARHGEF6):c.*1817dup rs751450350
NM_004840.3(ARHGEF6):c.*197GTT[1] rs770569536
NM_153252.5(BRWD3):c.*6025dup rs201004001

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