ClinVar Miner

List of variants in gene CANT1 reported as benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001159773.2(CANT1):c.159T>C (p.Ala53=) rs8077024 0.34524
NM_001159773.2(CANT1):c.*1440G>A rs4861 0.14246
NM_001159773.2(CANT1):c.-23+25G>A rs3744171 0.12298
NM_001159773.2(CANT1):c.*847C>T rs11891 0.12297
NM_001159773.2(CANT1):c.1056C>T (p.Asn352=) rs3803781 0.03451
NM_001159773.2(CANT1):c.*964A>G rs75126416 0.03342
NM_001159773.2(CANT1):c.*664T>C rs79189369 0.03215
NM_001159773.2(CANT1):c.*671T>C rs114125762 0.03215
NM_001159773.2(CANT1):c.*829G>A rs115856545 0.02343
NM_001159773.2(CANT1):c.*1093C>T rs8078860 0.00775
NM_001159773.2(CANT1):c.*1149C>T rs114706748 0.00568
NM_001159773.2(CANT1):c.*1476G>A rs73999357 0.00503
NM_001159773.2(CANT1):c.*1056T>C rs77565945 0.00109
NM_001159773.2(CANT1):c.*1732T>C rs184171534 0.00041
NM_001159773.2(CANT1):c.*570G>A rs8079368

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