RS397514560 PTEN

Health Risk Chr 10:87933151
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Macrocephaly-autism syndrome
PTEN hamartoma tumor syndrome
Diffuse pediatric-type high-grade glioma
H3-wildtype and IDH-wildtype
Macrocephaly-autism syndrome
PTEN hamartoma tumor syndrome
Diffuse pediatric-type high-grade glioma
H3-wildtype and IDH-wildtype
Other Variants in PTEN
rs121909218 rs121909219 rs121909220 rs121909221 rs121909222 rs121909223 rs587776666 rs121909224 rs587776667 rs1554898244
Ask Dr. Hemsworth about this variant