ClinVar Miner

List of variants in gene combination MYO5B, SNHG22 reported as benign for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_001080467.3(MYO5B):c.*308C>T rs555879 0.53747
NM_001080467.3(MYO5B):c.*965A>T rs72642495 0.20122
NM_001080467.3(MYO5B):c.4464G>A (p.Leu1488=) rs2276170 0.12248
NM_001080467.3(MYO5B):c.*1921G>C rs111319402 0.11314
NM_001080467.3(MYO5B):c.*979G>A rs74515646 0.08075
NM_001080467.3(MYO5B):c.*371T>C rs4127441 0.06808
NM_001080467.3(MYO5B):c.*707T>C rs12457962 0.06804
NM_001080467.3(MYO5B):c.*873G>A rs4638687 0.06800
NM_001080467.3(MYO5B):c.*2747A>C rs11876859 0.02257
NM_001080467.3(MYO5B):c.*3273G>A rs9947739 0.02247
NM_001080467.3(MYO5B):c.5062A>G (p.Met1688Val) rs112417235 0.02197
NM_001080467.3(MYO5B):c.5433A>C (p.Leu1811=) rs78657366 0.02050
NM_001080467.3(MYO5B):c.*1614T>C rs111994054 0.01125
NM_001080467.3(MYO5B):c.*1610G>C rs148887718 0.00836
NM_001080467.3(MYO5B):c.*1142A>C rs146397214 0.00739
NM_001080467.3(MYO5B):c.*1404T>C rs113054799 0.00736
NM_001080467.3(MYO5B):c.*1272A>C rs114133687 0.00732
NM_001080467.3(MYO5B):c.*2645T>G rs140855200 0.00732
NM_001080467.3(MYO5B):c.5048A>G (p.Lys1683Arg) rs9950781 0.00683
NM_001080467.3(MYO5B):c.*3368G>C rs9947614 0.00671
NM_001080467.3(MYO5B):c.*2283T>C rs59318525 0.00667
NM_001080467.3(MYO5B):c.*2293T>G rs57818618 0.00156
NM_001080467.3(MYO5B):c.*958T>C rs143115573 0.00108
NM_001080467.3(MYO5B):c.*400G>A rs144380641 0.00048
NM_001080467.3(MYO5B):c.*1671G>T rs9959610
NM_001080467.3(MYO5B):c.*2240A>C rs607552
NM_001080467.3(MYO5B):c.*99A>C rs11874243

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