ClinVar Miner

List of variants reported as pathogenic for synucleinopathy by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (15):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NC_000004.11:g.(?_90647315)_(90756828_?)dup
NC_000004.11:g.(?_90647315)_(90756838_?)dup
NC_000004.11:g.(?_90647779)_(90756818_?)dup
NM_000345.4(SNCA):c.136G>A (p.Glu46Lys) rs104893875
NM_000345.4(SNCA):c.157G>A (p.Ala53Thr) rs104893877
NM_000345.4(SNCA):c.89C>G (p.Ala30Gly) rs2110525413

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