ClinVar Miner

List of variants in gene ANO10, LOC129936579 studied for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_018075.5(ANO10):c.-104C>T rs6799022 0.01014
NM_018075.5(ANO10):c.-90C>T rs565644253 0.00916
NM_018075.5(ANO10):c.-83T>C rs760135054 0.00581
NM_018075.5(ANO10):c.-31G>C rs533146042 0.00347
NM_018075.5(ANO10):c.-74C>T rs886058482 0.00029
NM_018075.5(ANO10):c.-67C>T rs563565187 0.00028
NM_018075.4(ANO10):c.-140G>A rs886058485 0.00002
NM_018075.5(ANO10):c.-102C>A rs886058484 0.00001
NM_018075.5(ANO10):c.-95del rs886058483

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