RS121918649 SPTB
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
ANEMIA
PERINATAL HEMOLYTIC
FATAL OR NEAR-FATAL
Hereditary spherocytosis type 2
SPTB-related disorder
ANEMIA
PERINATAL HEMOLYTIC
FATAL OR NEAR-FATAL
Hereditary spherocytosis type 2
SPTB-related disorder
Other Variants in SPTB