ClinVar Miner

List of variants in gene combination MYO5B, SNHG22 reported as benign for Diarrhea with Microvillus Atrophy

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_001080467.3(MYO5B):c.*109del rs34922262 0.06499
NM_001080467.3(MYO5B):c.*1056del rs34780331

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