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Links from Gene

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNJ18
(P122S)
Single nucleotide variant
(missense variant)
Thyrotoxic periodic paralysis, susceptibility to, 2
GUncertain significance
KCNJ12, KCNJ18
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
KCNJ18
(R219C)
Single nucleotide variant
(missense variant)
Thyrotoxic periodic paralysis, susceptibility to, 2
GUncertain significance
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