RS886041216 NR2F1

Health Risk Chr 5:93585025
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What This Variant Does
"CLNSIG=5
Associated Conditions
Bosch-Boonstra-Schaaf optic atrophy syndrome
Inborn genetic diseases
Bosch-Boonstra-Schaaf optic atrophy syndrome
Inborn genetic diseases
Other Variants in NR2F1
rs587777274 rs587777275 rs587777276 rs587777277 rs863224903 rs886039714 rs778199728 rs886041738 rs1057519434 rs1057522318
Ask Dr. Hemsworth about this variant