RS1335777232 EBP

Health Risk Chr X:48524021
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Associated Conditions
Inborn genetic diseases
MEND syndrome
Chondrodysplasia punctata 2 X-linked dominant
Inborn genetic diseases
MEND syndrome
Chondrodysplasia punctata 2 X-linked dominant
Other Variants in EBP
rs104894798 rs104894799 rs104894800 rs1569479885 rs1569479901 rs1569480016 rs104894792 rs104894793 rs104894794 rs28935174
Ask Dr. Hemsworth about this variant