ClinVar Miner

List of variants in gene ALKBH8 reported as benign for carbohydrate metabolism disease

Included ClinVar conditions (301):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_138775.3(ALKBH8):c.720T>C (p.Asp240=) rs645056 0.76333
NM_138775.3(ALKBH8):c.878+31T>A rs589788 0.52394
NM_138775.3(ALKBH8):c.1288-3C>T rs654093 0.45699
NM_138775.3(ALKBH8):c.1030+9A>G rs12574614 0.24106
NM_138775.3(ALKBH8):c.772-72_772-71del rs5794554

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