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rs121908866(A;G)

From SNPedia
Carrier of a congenital hypothyroidism mutation; 3.3x higher risk for hypothyroidism
Is agenotype
ofrs121908866
GeneTSHR, LOC101928431, LOC101928462
Chromosome14
Position81,143,695
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;G) 3 Carrier of a congenital hypothyroidism mutation; 3.3x higher risk for hypothyroidism
(G;G) 0 common in clinvar

Unaffected in absence of a second TSHR gene mutation; see links and text via main rs-page