RS387906312 ALMS1

Health Risk Chr 2:73572649
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Alstrom syndrome
Retinal dystrophy
Cardiovascular phenotype
Bardet-Biedl syndrome
Alstrom syndrome
Retinal dystrophy
Cardiovascular phenotype
Bardet-Biedl syndrome
Other Variants in ALMS1
rs2104104085 rs193919338 rs387906313 rs193919339 rs193919340 rs397514576 rs398122991 rs398122992 rs398122993 rs398122994
Ask Dr. Hemsworth about this variant