RS786205509 RGS9

Health Risk Chr 17:65190194
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in RGS9
rs121908449 rs574696410 rs201026246 rs797044755 rs373346845 rs200798153 rs200492363 rs201997888 rs538728807 rs779441016
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