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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WNK1
Single nucleotide variant
(synonymous variant)
Pseudohypoaldosteronism type 2C
+2 more
GConflicting classifications of pathogenicity
WNK1
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
WNK1
Single nucleotide variant
(synonymous variant)
Pseudohypoaldosteronism type 2C
+2 more
GConflicting classifications of pathogenicity
WNK1
(K590R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
WNK1
(T665I)
Single nucleotide variant
(missense variant)
Neuropathy, hereditary sensory and autonomic, type 2A
+3 more
GBenign
WNK1
(A1277V +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GBenign/Likely benign
WNK1
Single nucleotide variant
(synonymous variant +1 more)
Pseudohypoaldosteronism type 2C
+4 more
GBenign/Likely benign
WNK1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
WNK1
(V966M +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
WNK1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
WNK1
Single nucleotide variant
(synonymous variant)
Neuropathy, hereditary sensory and autonomic, type 2A
+2 more
GUncertain significance
WNK1
(S1445N +3 more)
Single nucleotide variant
(missense variant)
WNK1-related condition
+5 more
GConflicting classifications of pathogenicity
WNK1
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
WNK1
Single nucleotide variant
(intron variant)
Inborn genetic diseases
+4 more
GBenign/Likely benign
WNK1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
WNK1
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
WNK1
(I2164L +3 more)
Single nucleotide variant
(missense variant)
Neuropathy, hereditary sensory and autonomic, type 2A
+5 more
GConflicting classifications of pathogenicity
WNK1
Single nucleotide variant
(synonymous variant)
Pseudohypoaldosteronism type 2C
+2 more
GConflicting classifications of pathogenicity
WNK1
(R2093H +3 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
WNK1
(S2460R +3 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
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