RS794727881 UPF3B

Health Risk Chr X:119841206
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What This Variant Does
"CLNSIG=5
Associated Conditions
Syndromic X-linked intellectual disability 14
UPF3B-associated intellectual disability
Inborn genetic diseases
Syndromic X-linked intellectual disability 14
UPF3B-associated intellectual disability
Inborn genetic diseases
Other Variants in UPF3B
rs1603370185 rs122468181 rs122468182 rs143538947 rs775715153 rs754982440 rs1064794254 rs1131691699 rs1556377028 rs187600102
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