ClinVar Miner

List of variants in gene YARS2 reported as uncertain significance for anemia (disease)

Included ClinVar conditions (258):
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Total variants: 18
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HGVS dbSNP
NM_001040436.2(YARS2):c.*24A>G rs368305831
NM_001040436.2(YARS2):c.*627A>T rs886049303
NM_001040436.2(YARS2):c.104C>A (p.Ala35Asp) rs149447502
NM_001040436.2(YARS2):c.1104-13dupA rs761612441
NM_001040436.2(YARS2):c.1241G>A (p.Arg414His) rs762786998
NM_001040436.2(YARS2):c.180G>A (p.Glu60=) rs137922867
NM_001040436.2(YARS2):c.234T>C (p.Cys78=) rs565102282
NM_001040436.2(YARS2):c.30C>T (p.Ser10=) rs886049305
NM_001040436.2(YARS2):c.327C>G (p.Ile109Met) rs886049304
NM_001040436.2(YARS2):c.456G>A (p.Ala152=) rs201940521
NM_001040436.2(YARS2):c.477C>T (p.Phe159=) rs774325742
NM_001040436.2(YARS2):c.535A>C (p.Lys179Gln) rs147630375
NM_001040436.2(YARS2):c.626A>G (p.Lys209Arg) rs541554381
NM_001040436.2(YARS2):c.819A>G (p.Leu273=) rs149781186
NM_001040436.2(YARS2):c.870T>C (p.Val290=) rs142067801
NM_001040436.2(YARS2):c.917T>C (p.Phe306Ser) rs376934259
NM_001040436.2(YARS2):c.930G>A (p.Pro310=) rs147551647
NM_001040436.2(YARS2):c.934G>C (p.Asp312His) rs190043383

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