ClinVar Miner

List of variants in gene RAB39B reported as uncertain significance for X-linked disease

Included ClinVar conditions (311):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_171998.4(RAB39B):c.*139_*142del rs1057515834
NM_171998.4(RAB39B):c.*1428T>G rs1057515831
NM_171998.4(RAB39B):c.*1452T>C
NM_171998.4(RAB39B):c.*1621del rs1057515830
NM_171998.4(RAB39B):c.*1728A>G rs1057515829
NM_171998.4(RAB39B):c.*1935G>A rs782447828
NM_171998.4(RAB39B):c.*1949_*1952CAAA[1] rs1057515828
NM_171998.4(RAB39B):c.*2100C>T rs1057515827
NM_171998.4(RAB39B):c.*2366G>A
NM_171998.4(RAB39B):c.*2551T>C
NM_171998.4(RAB39B):c.*339T>C rs781919581
NM_171998.4(RAB39B):c.*428C>T
NM_171998.4(RAB39B):c.*485T>G rs1057515833
NM_171998.4(RAB39B):c.*588A>G
NM_171998.4(RAB39B):c.*659_*660insATA rs1057515832
NM_171998.4(RAB39B):c.*65A>G rs900423679
NM_171998.4(RAB39B):c.-61G>C rs898651947
NM_171998.4(RAB39B):c.-62C>A
NM_171998.4(RAB39B):c.-84C>G
NM_171998.4(RAB39B):c.273T>C (p.Ile91=) rs1057515836

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