RS397514753 TMEM231

Health Risk Chr 16:75542602
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Meckel syndrome
type 11
Meckel-Gruber syndrome
TMEM231-related disorder
Joubert syndrome 20
Meckel syndrome
type 11
Meckel-Gruber syndrome
TMEM231-related disorder
Joubert syndrome 20
Other Variants in TMEM231
rs397514609 rs200799769 rs397514754 rs370607340 rs149888762 rs886039807 rs202215735 rs377440297 rs376300743 rs199776253
Ask Dr. Hemsworth about this variant