ClinVar Miner

List of variants in gene RARS2 reported as uncertain significance by GeneDx

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_020320.5(RARS2):c.773G>A (p.Arg258His) rs145297855 0.00044
NM_020320.5(RARS2):c.1637C>T (p.Pro546Leu) rs142348911 0.00026
NM_020320.5(RARS2):c.1108G>C (p.Glu370Gln) rs138490776 0.00023
NM_020320.5(RARS2):c.754T>A (p.Tyr252Asn) rs140692271 0.00018
NM_020320.5(RARS2):c.1413C>G (p.His471Gln) rs187815721 0.00016
NM_020320.5(RARS2):c.1366C>T (p.Arg456Cys) rs147844153 0.00011
NM_020320.5(RARS2):c.1253A>G (p.Lys418Arg) rs771658534 0.00008
NM_020320.5(RARS2):c.1327T>C (p.Ser443Pro) rs775295739 0.00006
NM_020320.5(RARS2):c.323A>G (p.Asp108Gly) rs750490956 0.00005
NM_020320.5(RARS2):c.5C>T (p.Ala2Val) rs760114539 0.00004
NM_020320.5(RARS2):c.916G>A (p.Asp306Asn) rs781646725 0.00003
NM_020320.5(RARS2):c.1442A>G (p.Tyr481Cys) rs775657290 0.00002
NM_020320.5(RARS2):c.152A>G (p.Glu51Gly) rs863224185 0.00002
NM_020320.5(RARS2):c.34C>G (p.Gln12Glu) rs368985469 0.00002
NM_020320.5(RARS2):c.970A>G (p.Thr324Ala) rs774506039 0.00002
NM_020320.5(RARS2):c.1086G>T (p.Lys362Asn) rs200101535 0.00001
NM_020320.5(RARS2):c.1555A>G (p.Arg519Gly) rs375989272 0.00001
NM_020320.5(RARS2):c.1678C>T (p.Arg560Cys) rs562472225 0.00001
NM_020320.5(RARS2):c.1708C>T (p.Leu570Phe) rs144242932 0.00001
NM_020320.5(RARS2):c.1724dup (p.Cys576fs) rs863224184 0.00001
NM_020320.5(RARS2):c.28G>A (p.Ala10Thr) rs755340864 0.00001
NM_020320.5(RARS2):c.887C>T (p.Thr296Met) rs374274799 0.00001
NM_020320.5(RARS2):c.-1C>G rs746862871
NM_020320.5(RARS2):c.1305+20T>C rs1057518531
NM_020320.5(RARS2):c.1439G>A (p.Gly480Glu) rs760844669
NM_020320.5(RARS2):c.1516G>A (p.Asp506Asn)
NM_020320.5(RARS2):c.1518C>A (p.Asp506Glu) rs754538094
NM_020320.5(RARS2):c.1567A>G (p.Ser523Gly) rs2127993935
NM_020320.5(RARS2):c.1651-12T>G rs769530438
NM_020320.5(RARS2):c.1654A>G (p.Arg552Gly) rs2127985828
NM_020320.5(RARS2):c.1679G>T (p.Arg560Leu)
NM_020320.5(RARS2):c.19C>T (p.Arg7Cys) rs201693843
NM_020320.5(RARS2):c.212A>G (p.Lys71Arg)
NM_020320.5(RARS2):c.407T>C (p.Val136Ala) rs1057519014
NM_020320.5(RARS2):c.473A>G (p.Lys158Arg) rs1554196985
NM_020320.5(RARS2):c.4G>A (p.Ala2Thr)
NM_020320.5(RARS2):c.613G>T (p.Val205Phe)
NM_020320.5(RARS2):c.736G>T (p.Asp246Tyr)
NM_020320.5(RARS2):c.757A>G (p.Ile253Val) rs863224179
NM_020320.5(RARS2):c.772-3del rs368859792
NM_020320.5(RARS2):c.772-4_772-3del rs368859792
NM_020320.5(RARS2):c.775C>G (p.Leu259Val) rs2128057909
NM_020320.5(RARS2):c.818G>T (p.Arg273Leu) rs139721632

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