rs33951465(T;T)

common in complete genomics

Is a	genotype
of	rs33951465
Gene	HBB
Chromosome	11
Position	5,226,947
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;T)	3	Carrier of a hemoglobin beta-thalassemia mutation
(T;T)	0	common in complete genomics
(TG;TG)	0	common in clinvar