RS104894914 OPN1MW

Health Risk Chr X:154191715 snv missense variant
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What This Variant Does
"middle European ancestry, suggesting a founder effect. fairly common (2&#37
Associated Conditions
Cone monochromatism
Deuteranomaly
Cone monochromatism
Deuteranomaly
Population Frequencies
gnomAD ALL
100%
Other Variants in OPN1MW
rs104894916 rs724159983 rs104894915 rs267606927 rs2148787747
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