RS776519022 CRBN

Health Risk Chr 3:3179661
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CRBN
rs121918368 rs797045036 rs373145132 rs78564552 rs541404259 rs1575079076 rs1575094649 rs1226252969 rs1706807912 rs1302797003
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