ClinVar Miner

List of variants in gene GARS1 reported as likely benign by GeneDx

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Gene type:
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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_002047.2(GARS1):c.-205C>T rs17159262 0.03007
NM_002047.4(GARS1):c.1359+97A>G rs2709772 0.01406
NM_002047.4(GARS1):c.223-132G>A rs117505203 0.01238
NC_000007.14:g.30634188C>T rs117407393 0.01138
NM_002047.4(GARS1):c.223-166G>A rs2240501 0.01088
NM_002047.4(GARS1):c.881+70T>C rs114018913 0.01039
NM_002047.4(GARS1):c.881+240A>G rs112431911 0.00714
NM_002047.2(GARS1):c.-225G>A rs148593022 0.00641
NM_002047.4(GARS1):c.1467+113G>A rs57305857 0.00598
NM_002047.4(GARS1):c.*67C>G rs142498676 0.00506
NM_002047.4(GARS1):c.1810-107T>G rs115985185 0.00438
NM_002047.2(GARS1):c.-177T>C rs78980639 0.00437
NC_000007.14:g.30594476T>C rs145875816 0.00416
NM_002047.4(GARS1):c.1195-47T>C rs145902909 0.00412
NM_002047.4(GARS1):c.1700-85G>A rs575217668 0.00383
NM_002047.4(GARS1):c.803C>T (p.Thr268Ile) rs2230310 0.00357
NM_002047.2(GARS1):c.-85C>A rs777045330 0.00243
NM_002047.4(GARS1):c.1420C>A (p.Arg474=) rs113958280 0.00210
NM_002047.4(GARS1):c.1810-199G>A rs117100393 0.00163
NM_002047.4(GARS1):c.1962C>T (p.Ile654=) rs201927627 0.00120
NM_002047.4(GARS1):c.699C>T (p.Val233=) rs187937286 0.00063
NM_002047.4(GARS1):c.428-17C>T rs370452042 0.00040
NM_002047.4(GARS1):c.1032-15C>T rs201868189 0.00037
NM_002047.4(GARS1):c.1904-18T>C rs41275991 0.00036
NM_002047.4(GARS1):c.675G>A (p.Leu225=) rs369203473 0.00033
NM_002047.4(GARS1):c.253A>G (p.Lys85Glu) rs200294578 0.00029
NM_002047.4(GARS1):c.1100A>G (p.Asn367Ser) rs192443850 0.00024
NM_002047.4(GARS1):c.51G>A (p.Leu17=) rs202117737 0.00023
NM_002047.4(GARS1):c.408A>G (p.Gln136=) rs200279483 0.00021
NM_002047.4(GARS1):c.428-13T>A rs373782750 0.00013
NM_002047.4(GARS1):c.236G>A (p.Arg79Gln) rs369466037 0.00011
NM_002047.4(GARS1):c.1809+14T>C rs367739730 0.00010
NM_002047.4(GARS1):c.270C>T (p.Asp90=) rs369898799 0.00009
NM_002047.4(GARS1):c.1716G>A (p.Pro572=) rs370608239 0.00008
NM_002047.4(GARS1):c.1149C>T (p.Ser383=) rs369389062 0.00007
NM_002047.4(GARS1):c.1852G>A (p.Val618Ile) rs369894731 0.00006
NM_002047.4(GARS1):c.764C>T (p.Ala255Val) rs765478968 0.00006
NM_002047.4(GARS1):c.1904-19del rs745958570 0.00005
NM_002047.4(GARS1):c.325-9C>G rs770645408 0.00005
NM_002047.4(GARS1):c.1158C>T (p.Ser386=) rs373576697 0.00004
NM_002047.4(GARS1):c.1754T>C (p.Met585Thr) rs374378925 0.00004
NM_002047.4(GARS1):c.1923T>C (p.His641=) rs182542046 0.00003
NM_002047.4(GARS1):c.262C>G (p.Gln88Glu) rs201728920 0.00003
NM_002047.4(GARS1):c.69G>A (p.Arg23=) rs762624758 0.00003
NM_002047.4(GARS1):c.-6A>G rs747409671 0.00002
NM_002047.4(GARS1):c.1553A>G (p.Tyr518Cys) rs753947676 0.00002
NM_002047.4(GARS1):c.271G>A (p.Val91Ile) rs374616031 0.00002
NM_002047.4(GARS1):c.1031+9del rs746178135 0.00001
NM_002047.4(GARS1):c.1700-17T>C rs775676664 0.00001
NM_002047.4(GARS1):c.492C>G (p.Thr164=) rs368297381 0.00001
NM_002047.4(GARS1):c.531G>A (p.Glu177=) rs759865366 0.00001
NM_002047.4(GARS1):c.*51dup rs70983380
NM_002047.4(GARS1):c.-40C>A rs775425723
NM_002047.4(GARS1):c.1171C>T (p.Arg391Cys) rs370057212
NM_002047.4(GARS1):c.1360-322del rs749336250
NM_002047.4(GARS1):c.1578C>T (p.Tyr526=) rs371268919
NM_002047.4(GARS1):c.1614-4G>A rs376324026
NM_002047.4(GARS1):c.1614-4G>C rs376324026
NM_002047.4(GARS1):c.1700-13A>T rs762966640
NM_002047.4(GARS1):c.325-292G>T rs147169899
NM_002047.4(GARS1):c.366A>G (p.Ala122=) rs1057521413
NM_002047.4(GARS1):c.569+8C>A rs1554337181
NM_002047.4(GARS1):c.658+14T>C rs1210407173
NM_002047.4(GARS1):c.93G>A (p.Leu31=) rs2529438

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