RS797044911 NFIX

Health Risk Chr 19:13025354
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Malan overgrowth syndrome
Marshall-Smith syndrome
Inborn genetic diseases
Malan overgrowth syndrome
Marshall-Smith syndrome
Other Variants in NFIX
rs387907253 rs398122869 rs398122870 rs398122871 rs398122872 rs398122873 rs398122874 rs398122875 rs398122876 rs387907254
Ask Dr. Hemsworth about this variant