RS137853057 PRKN

Health Risk Chr 6:162201182
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What This Variant Does
"c.483A&gt
Associated Conditions
Autosomal recessive juvenile Parkinson disease 2
Autosomal recessive juvenile Parkinson disease 2
Other Variants in PRKN
rs137853054 rs137853055 rs137853056 rs137853058 rs137853059 rs34424986 rs137853060 rs397518439 rs56092260 rs397514694
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