ClinVar Miner

List of variants reported as uncertain significance for Parkinson disease by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_022089.4(ATP13A2):c.*130C>T rs189334432
NM_022089.4(ATP13A2):c.1039+6C>T rs565724504
NM_022089.4(ATP13A2):c.1542+3G>A rs747456787
NM_022089.4(ATP13A2):c.2640C>T (p.Ala880=) rs567287489
NM_022089.4(ATP13A2):c.2746G>A (p.Val916Met) rs768674400
NM_022089.4(ATP13A2):c.2972G>A (p.Arg991Gln)
NM_022089.4(ATP13A2):c.3405+9C>T rs374766933

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