RS397518483 RARB

Health Risk Chr 3:25596428
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microphthalmia
syndromic 12
Inborn genetic diseases
Intellectual disability
autosomal dominant 48
Microphthalmia
syndromic 12
Microphthalmia
syndromic 12
Inborn genetic diseases
Intellectual disability
autosomal dominant 48
Microphthalmia
syndromic 12
Other Variants in RARB
rs2529761251 rs1701836507 rs201295268 rs2125325458 rs2529457082 rs2529761078 rs2529826385 rs551369280 rs2529761773 rs1701834292
Ask Dr. Hemsworth about this variant