ClinVar Miner

List of variants in gene EIF2B2, MLH3 studied for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_014239.4(EIF2B2):c.*180G>C rs4556 0.45760
NM_001040108.2(MLH3):c.*3148A>G rs108621 0.42508
NM_001040108.2(MLH3):c.*2965C>T rs10134636 0.03135
NM_014239.4(EIF2B2):c.*3G>C rs112087431 0.01958
NM_014239.4(EIF2B2):c.*56C>T rs116393177 0.01153
NM_001040108.2(MLH3):c.*3140C>T rs77514025 0.00950

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