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rs1049296(T;T)

From SNPedia

C2 transferrin subtype; very slightly higher risk for Alzheimers
Is agenotype
ofrs1049296
GeneTF
Chromosome3
Position133,775,510
mentionedby
Magnitude1.2
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