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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD1
Single nucleotide variant
(intron variant)
Pilarowski-Bjornsson syndrome
GUncertain significance
CHD1
(S1183G)
Single nucleotide variant
(missense variant +1 more)
Pilarowski-Bjornsson syndrome
GUncertain significance
CHD1
(R785C)
Single nucleotide variant
(missense variant +1 more)
Pilarowski-Bjornsson syndrome
GUncertain significance
CHD1
(N227D)
Single nucleotide variant
(missense variant +1 more)
Pilarowski-Bjornsson syndrome
GUncertain significance
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