RS104893878 SNCA

Health Risk Chr 4:89835580
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What This Variant Does
"c.88G&gt
Associated Conditions
Autosomal dominant Parkinson disease 1
Autosomal dominant Parkinson disease 1
Other Variants in SNCA
rs104893877 rs104893875 rs431905511 rs527798413 rs532025477 rs144758871 rs149401968 rs1739238968 rs542171324 rs2110525413
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