rs920590

Parent Gene: CSGALNACT1, INTS10

Importance: 3
Less common allele: C = 44%
More common allele: T = 56%
My Genotype: Log In
Risk Allele: C, C

Disease/Trait: Acute Lymphoblastic Leukemia

The C allele of rs920590 is reported to be associated with Acute Lymphoblastic Leukemia (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Acute lymphoblastic leukemia (childhood) (ETV6-RUNX1 positive, Northern European).

Disease/Trait: Acute Lymphoblastic Leukemia

The C allele of rs920590 is reported to be associated with Acute Lymphoblastic Leukemia (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Acute lymphoblastic leukemia (childhood) (ETV6-RUNX1 positive).