rs1049296(T;T)

C2 transferrin subtype; very slightly higher risk for Alzheimers

Is a	genotype
of	rs1049296
Gene	TF
Chromosome	3
Position	133,775,510
mentioned	by

Magnitude

1.2

Geno	Mag	Summary
(C;C)	0	C1 subtype of transferrin; common in clinvar
(C;T)	1.1	Heterozygote carrying both C1 and C2 transferrin subtypes; very slightly higher risk for Alzheimers
(T;T)	1.2	C2 transferrin subtype; very slightly higher risk for Alzheimers