rs1800454(A;G)

carrier

Is a	genotype
of	rs1800454
Gene	TAP2
Chromosome	6
Position	32,832,635
Merged from	Rs104893997
mentioned	by

Magnitude

1.3

Geno	Mag	Summary
(A;A)	1.5	affected
(A;G)	1.3	carrier
(G;G)	0	normal

Since this comes from omim, it's supposed to be a rare disorder, but HapMap shows that variation is common