ClinVar Miner

List of variants reported as risk factor for Pheochromocytoma, susceptibility to

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Total variants: 9
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HGVS dbSNP
NM_002382.5(MAX):c.187del (p.Ile63fs) rs1566600827
NM_002382.5(MAX):c.1A>G (p.Met1Val) rs387906649
NM_002382.5(MAX):c.223C>T (p.Arg75Ter) rs387906650
NM_002382.5(MAX):c.295+1G>A rs786203385
NM_002382.5(MAX):c.97C>T (p.Arg33Ter) rs387906651
NM_017849.3(TMEM127):c.149dup (p.Pro51fs) rs121908817
NM_017849.3(TMEM127):c.245-1G>T rs121908821
NM_017849.3(TMEM127):c.410-2A>C rs121908826
NM_017849.3(TMEM127):c.475C>T (p.Gln159Ter) rs121908830

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