RS786205474 AICDA

Health Risk Chr 12:8605473
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Hyper-IgM syndrome type 2
Hyper-IgM syndrome type 2
Other Variants in AICDA
rs104894324 rs104894325 rs104894321 rs104894322 rs104894323 rs104894327 rs387906328 rs387906329 rs193922703 rs193922704
Ask Dr. Hemsworth about this variant