ClinVar Miner

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

Included ClinVar conditions (32):
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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_022089.4(ATP13A2):c.*124C>T rs15786
NM_022089.4(ATP13A2):c.1005C>T (p.Ala335=) rs56290406
NM_022089.4(ATP13A2):c.1128C>T (p.Cys376=) rs148970081
NM_022089.4(ATP13A2):c.1195+10G>A rs55689004
NM_022089.4(ATP13A2):c.1195+9C>T rs117758987
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.1815C>T (p.Pro605=) rs2076603
NM_022089.4(ATP13A2):c.2093T>C (p.Val698Ala) rs61734958
NM_022089.4(ATP13A2):c.2367C>T (p.Leu789=) rs140048110
NM_022089.4(ATP13A2):c.2637C>T (p.Gly879=) rs9435662
NM_022089.4(ATP13A2):c.2724G>A (p.Ser908=) rs79724242
NM_022089.4(ATP13A2):c.2790G>A (p.Ser930=) rs3738815
NM_022089.4(ATP13A2):c.2970G>A (p.Val990=) rs761421
NM_022089.4(ATP13A2):c.3084-3C>T rs7531163
NM_022089.4(ATP13A2):c.3144C>G (p.Thr1048=) rs56126202
NM_022089.4(ATP13A2):c.3192C>T (p.Ala1064=) rs9435659
NM_022089.4(ATP13A2):c.3516G>A (p.Pro1172=) rs3170740
NM_022089.4(ATP13A2):c.453C>T (p.Ser151=) rs55979991
NM_022089.4(ATP13A2):c.881G>A (p.Arg294Gln) rs56367069

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