ClinVar Miner

List of variants reported as pathogenic for Bruck syndrome 1 by OMIM

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_021939.4(FKBP10):c.337G>A (p.Glu113Lys) rs397514674 0.00001
NM_021939.4(FKBP10):c.344G>A (p.Arg115Gln) rs387906960 0.00001
NM_021939.4(FKBP10):c.1016_1023dup (p.Thr342fs)
NM_021939.4(FKBP10):c.1271_1272delinsA (p.Ala424fs) rs397509383
NM_021939.4(FKBP10):c.1276dup (p.Gln426fs) rs1567856056
NM_021939.4(FKBP10):c.743dup (p.Gln249fs) rs1555616552
NM_021939.4(FKBP10):c.831dup (p.Gly278fs) rs137853883
NM_021939.4(FKBP10):c.877_879del (p.Tyr293del) rs869320752

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