ClinVar Miner

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

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_171998.4(RAB39B):c.*1006A>G rs138077054
NM_171998.4(RAB39B):c.*1040C>T rs185958813
NM_171998.4(RAB39B):c.*1079A>C rs147409916
NM_171998.4(RAB39B):c.*1347C>T rs17052027
NM_171998.4(RAB39B):c.*1580C>G rs115301020
NM_171998.4(RAB39B):c.*1656= rs3105275
NM_171998.4(RAB39B):c.*1813C>A rs17052030
NM_171998.4(RAB39B):c.*1945A>T rs145867198
NM_171998.4(RAB39B):c.*282G>T rs147213132
NM_171998.4(RAB39B):c.543A>G (p.Thr181=) rs369970931

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