RS587777606 BSCL2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Severe neurodegenerative syndrome with lipodystrophy
Congenital generalized lipodystrophy type 2
Charcot-Marie-Tooth disease type 2
Berardinelli-Seip congenital lipodystrophy
Severe neurodegenerative syndrome with lipodystrophy
Congenital generalized lipodystrophy type 2
Charcot-Marie-Tooth disease type 2
Berardinelli-Seip congenital lipodystrophy
Other Variants in BSCL2