ClinVar Miner

List of variants in gene combination FBXO11, MSH6 reported as benign for not provided

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Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_001190274.2(FBXO11):c.*1173A>T rs2020906 0.00645
NM_001190274.2(FBXO11):c.2436G>A (p.Val812=) rs148676301 0.00029
NM_001190274.2(FBXO11):c.2491A>G (p.Ser831Gly) rs200771165 0.00024
NM_001190274.2(FBXO11):c.2654+17C>G rs374404244 0.00010
NM_001190274.2(FBXO11):c.2555+5C>T rs368811481 0.00005
NM_001190274.2(FBXO11):c.2458A>G (p.Met820Val) rs747122948 0.00004
NM_001190274.2(FBXO11):c.2555+4A>C rs1363141549 0.00001
NM_001190274.2(FBXO11):c.2699C>G (p.Thr900Arg) rs780870758 0.00001
GRCh37/hg19 2p16.3(chr2:47833880-48131936)x3
NM_001190274.2(FBXO11):c.2556-3T>C
NM_001190274.2(FBXO11):c.2655-19G>T

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