ClinVar Miner

List of variants in gene combination DNM1L, YARS2 reported as likely benign for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_001040436.3(YARS2):c.*162A>G rs11052215
NM_001040436.3(YARS2):c.*191T>C rs144235100
NM_001040436.3(YARS2):c.*209G>C rs10844337
NM_001040436.3(YARS2):c.*406C>T rs145618550
NM_001040436.3(YARS2):c.*643G>A rs11052214
NM_001040436.3(YARS2):c.1356A>G (p.Gln452=) rs148729348
NM_012062.5(DNM1L):c.*1156G>C rs148183516
NM_012062.5(DNM1L):c.*1213G>T rs11052213
NM_012062.5(DNM1L):c.*1242G>A rs10844336
NM_012062.5(DNM1L):c.*1415T>C rs114366772
NM_012062.5(DNM1L):c.*21G>C rs1059422
NM_012062.5(DNM1L):c.*22A>T rs3200103
NM_012062.5(DNM1L):c.*271C>G rs1020670
NM_012062.5(DNM1L):c.*393A>C rs77298476
NM_012062.5(DNM1L):c.*600C>T rs3600
NM_012062.5(DNM1L):c.*744A>T rs1971911

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