ClinVar Miner

List of variants in gene SIM1 reported as likely benign for Prader-Willi syndrome

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_005068.2(SIM1):c.*113A>T rs41318039
NM_005068.2(SIM1):c.*1453G>T rs13201004
NM_005068.2(SIM1):c.*375C>T rs114523604
NM_005068.2(SIM1):c.*51G>A rs55805997
NM_005068.2(SIM1):c.-127T>C rs41315244

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