ClinVar Miner

List of variants in gene ATP13A2 reported as likely benign for Parkinson disease

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_022089.4(ATP13A2):c.*120A>T rs41273151
NM_022089.4(ATP13A2):c.*243A>C rs777596557
NM_022089.4(ATP13A2):c.*251A>G rs535432261
NM_022089.4(ATP13A2):c.1005C>T (p.Ala335=) rs56290406
NM_022089.4(ATP13A2):c.106-8G>A rs200587951
NM_022089.4(ATP13A2):c.1195+10G>A rs55689004
NM_022089.4(ATP13A2):c.1195+7G>A rs1407939803
NM_022089.4(ATP13A2):c.1195+9C>T rs117758987
NM_022089.4(ATP13A2):c.1203C>T (p.Cys401=) rs148026506
NM_022089.4(ATP13A2):c.132A>G (p.Pro44=) rs200816691
NM_022089.4(ATP13A2):c.1614C>T (p.Pro538=) rs56351817
NM_022089.4(ATP13A2):c.1617G>T (p.Leu539=) rs61739752
NM_022089.4(ATP13A2):c.2348G>A (p.Arg783Gln) rs137955309
NM_022089.4(ATP13A2):c.2610-9T>C rs376189607
NM_022089.4(ATP13A2):c.2619G>C (p.Val873=) rs199994961
NM_022089.4(ATP13A2):c.3144C>G (p.Thr1048=) rs56126202
NM_022089.4(ATP13A2):c.3297C>T (p.Pro1099=) rs756650754
NM_022089.4(ATP13A2):c.777C>T (p.Tyr259=) rs780133367
NM_022089.4(ATP13A2):c.844A>T (p.Ser282Cys) rs538497077
NM_022089.4(ATP13A2):c.951C>T (p.Cys317=) rs148391179

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