ClinVar Miner

List of variants in gene combination MIR4741, RBBP8 reported as uncertain significance for Seckel syndrome

Included ClinVar conditions (16):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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NM_002894.3(RBBP8):c.-225G>C rs570452407
NM_002894.3(RBBP8):c.-250G>A rs115479920
NM_002894.3(RBBP8):c.-253G>A rs886053655
NM_002894.3(RBBP8):c.-265C>T rs886053654
NM_002894.3(RBBP8):c.-269C>T rs886053653

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