RS387907186 SF3B4

Health Risk Chr 1:149923670
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What This Variant Does
"CLNSIG=5
Associated Conditions
Nager syndrome
Inborn genetic diseases
Nager syndrome
Inborn genetic diseases
Nager syndrome
Inborn genetic diseases
Nager syndrome
Inborn genetic diseases
Other Variants in SF3B4
rs387907185 rs797045125 rs397515324 rs797044869 rs797045121 rs797045122 rs797045123 rs797045124 rs782357237 rs797045126
Ask Dr. Hemsworth about this variant