RS200799769 TMEM231

Health Risk Chr 16:75542641
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What This Variant Does
"CLNSIG=5
Associated Conditions
Joubert syndrome 20
Meckel syndrome
type 11
Inborn genetic diseases
Joubert syndrome and related disorders
TMEM231-related disorder
Joubert syndrome 20
Meckel syndrome
type 11
Inborn genetic diseases
Joubert syndrome and related disorders
TMEM231-related disorder
Other Variants in TMEM231
rs397514609 rs397514753 rs397514754 rs370607340 rs149888762 rs886039807 rs202215735 rs377440297 rs376300743 rs199776253
Ask Dr. Hemsworth about this variant