ClinVar Miner

List of variants reported as benign for TH-deficient dopa-responsive dystonia by Genome-Nilou Lab

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_000360.4(TH):c.1048-110A>C rs4072823 0.99112
NM_000360.4(TH):c.695+99G>A rs7925924 0.91868
NM_000360.4(TH):c.696-126C>G rs7942881 0.91851
NM_000360.4(TH):c.1105-78A>G rs6578990 0.91463
NM_000360.4(TH):c.91-54A>G rs7925375 0.69448
NM_000360.4(TH):c.577-22C>T rs4074905 0.62210
NM_000360.4(TH):c.1334+127T>C rs2070762 0.42979
NM_000360.4(TH):c.241G>A (p.Val81Met) rs6356 0.31555
NM_000360.4(TH):c.977+8C>G rs12419447 0.27597
NM_000360.4(TH):c.720G>A (p.Lys240=) rs6357 0.23916
NM_000360.4(TH):c.313-88G>A rs4930043 0.22256
NM_000360.4(TH):c.487+3G>A rs11042950 0.00795
NM_000360.4(TH):c.267G>A (p.Arg89=) rs76240471 0.00521
NM_000360.4(TH):c.51C>T (p.Ala17=) rs199645400 0.00013
NM_000360.4(TH):c.696-138G>A rs7925784

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