ClinVar Miner

List of variants reported as likely benign for Meacham syndrome by Illumina Laboratory Services, Illumina

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.*897G>C rs5030324 0.00520
NM_024426.6(WT1):c.*542G>A rs142726499 0.00380
NM_024426.6(WT1):c.181C>A (p.Arg61=) rs2234581 0.00270
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427 0.00197
NM_024426.6(WT1):c.*138G>A rs111351882 0.00165
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135 0.00036
NM_024426.6(WT1):c.785G>A (p.Gly262Asp) rs372225738 0.00006
NM_024426.6(WT1):c.587G>A (p.Gly196Asp) rs753112302 0.00002
NM_024426.6(WT1):c.887+4G>A rs778673400 0.00002
NM_024426.6(WT1):c.1198T>C (p.Tyr400His) rs746353651 0.00001
NM_024426.6(WT1):c.1568G>A (p.Ter523=) rs148856160 0.00001

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