RS137852970 BSCL2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital generalized lipodystrophy type 2
Inborn genetic diseases
Neuronopathy
distal hereditary motor
type 5C
Berardinelli-Seip congenital lipodystrophy
Congenital generalized lipodystrophy type 2
Inborn genetic diseases
Neuronopathy
distal hereditary motor
type 5C
Berardinelli-Seip congenital lipodystrophy
Other Variants in BSCL2