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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IL6, IL6-AS1
+1 more
(A17D +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
IL6, IL6-AS1
+1 more
(Q33H +1 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GLikely benign
IL6
(M19I +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
IL6
(N160K +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
IL6
(R184T +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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