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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3802-40C>G	rs3136367	0.73398
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
NM_000179.3(MSH6):c.3647-6T>C	rs182871847
NM_000179.3(MSH6):c.4002-8A>T	rs778957100
NM_000179.3(MSH6):c.4068_4071dup (p.Lys1358delinsAspTer)	rs55740729
NM_001190274.2(FBXO11):c.2556-3T>C
NM_001190274.2(FBXO11):c.2655-19G>T

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