ClinVar Miner

List of variants in gene ARX reported as likely benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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NM_139058.3(ARX):c.1033C>A (p.Arg345=) rs1601948273
NM_139058.3(ARX):c.1269C>T (p.His423=) rs794727656
NM_139058.3(ARX):c.1448+9C>A rs759009252
NM_139058.3(ARX):c.1488C>T (p.Thr496=) rs773666007
NM_139058.3(ARX):c.1515A>G (p.Thr505=) rs398124509
NM_139058.3(ARX):c.1599C>G (p.Ala533=) rs1057523196
NM_139058.3(ARX):c.166A>G (p.Ser56Gly) rs144098296
NM_139058.3(ARX):c.264G>A (p.Leu88=) rs1556056513
NM_139058.3(ARX):c.558G>T (p.Pro186=) rs748764628
NM_139058.3(ARX):c.602C>A (p.Pro201Gln) rs1484238484
NM_139058.3(ARX):c.611G>A (p.Arg204His) rs755745002
NM_139058.3(ARX):c.642C>A (p.Ala214=) rs997439358
NM_139058.3(ARX):c.663C>G (p.Thr221=) rs1006404746
NM_139058.3(ARX):c.678C>T (p.Asp226=) rs764730866
NM_139058.3(ARX):c.708T>C (p.Asp236=) rs763458576
NM_139058.3(ARX):c.807C>T (p.Ala269=) rs587783205
NM_139058.3(ARX):c.855G>A (p.Glu285=) rs139301257
NM_139058.3(ARX):c.921C>A (p.Gly307=) rs398124519

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