ClinVar Miner

List of variants reported as benign for X-linked disease by Integrated Genetics/Laboratory Corporation of America

Included ClinVar conditions (311):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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NM_001110792.2(MECP2):c.1108G>A (p.Ala370Thr) rs147017239
NM_001110792.2(MECP2):c.1197C>T (p.Pro399=) rs61750246
NM_001110792.2(MECP2):c.1269C>T (p.Ser423=) rs3027928
NM_001110792.2(MECP2):c.626C>T (p.Thr209Met) rs61749714
NM_001110792.2(MECP2):c.813C>T (p.Ala271=) rs1042870
NM_001110792.2(MECP2):c.855G>T (p.Gly285=) rs61750245
NM_004992.3(MECP2):c.378-20C>G rs368684221

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