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rs1800454(A;G)

From SNPedia

carrier
Is agenotype
ofrs1800454
GeneTAP2
Chromosome6
Position32,832,635
Merged fromRs104893997
mentionedby
Magnitude1.3
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