RS200210006 GRM6

Health Risk Chr 5:178981667
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Associated Conditions
Retinal dystrophy
Inborn genetic diseases
Retinal dystrophy
Inborn genetic diseases
Other Variants in GRM6
rs62638214 rs62638624 rs62638202 rs62638197 rs121434304 rs143491269 rs62638619 rs281865186 rs61731186 rs748979061
Ask Dr. Hemsworth about this variant