List of variants reported as not provided for MELAS syndrome by GeneReviews

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CO1):m.7023G>A	rs2124593767
NC_012920.1(MT-CO3):m.9957T>C	rs1556423753
NC_012920.1(MT-CYB):m.14864T>C
NC_012920.1(MT-CYB):m.583G>A	rs118203885
NC_012920.1(MT-ND1):m.1644G>A	rs587776441
NC_012920.1(MT-ND1):m.3481G>A	rs587776433
NC_012920.1(MT-ND1):m.3697G>A	rs199476122
NC_012920.1(MT-ND1):m.3946G>A	rs199476123
NC_012920.1(MT-ND1):m.3949T>C	rs199476124
NC_012920.1(MT-ND5):m.12770A>G	rs267606894
NC_012920.1(MT-ND5):m.13042G>A	rs267606898
NC_012920.1(MT-ND5):m.13084A>T	rs267606896
NC_012920.1(MT-ND5):m.13513G>A	rs267606897
NC_012920.1(MT-ND5):m.13514A>G	rs587776440
NC_012920.1(MT-ND5):m.13528A>G	rs55882959
NC_012920.1(MT-ND6):m.14453G>A	rs199476107
NC_012920.1(MT-TH):m.12146A>G	rs2124597054
NC_012920.1(MT-TH):m.12147G>A	rs121434474
NC_012920.1(MT-TK):m.8296A>G	rs118192102
NC_012920.1(MT-TK):m.8316T>C
NC_012920.1(MT-TL1):m.3243A>G	rs199474657
NC_012920.1(MT-TL1):m.3252A>G	rs199474661
NC_012920.1(MT-TL1):m.3256C>T	rs199474659
NC_012920.1(MT-TL1):m.3260A>G	rs199474663
NC_012920.1(MT-TL1):m.3271T>C	rs199474658
NC_012920.1(MT-TL1):m.3291T>C	rs869312463
NC_012920.1(MT-TL2):m.12299A>C
NC_012920.1(MT-TQ):m.4332G>A	rs199476141
NC_012920.1(MT-TS1):m.7512T>C	rs199474817
NC_012920.1(MT-TS2):m.12207G>A	rs118203889
NC_012920.1(MT-TV):m.1642G>A	rs2124591032
NC_012920.1(MT-TW):m.5521G>A	rs199474673

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