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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALMS1
(Y680C +1 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
ALMS1
(K2037N +1 more)
Single nucleotide variant
(missense variant)
Alstrom syndrome
GUncertain significance
ALMS1
(K2101I +1 more)
Single nucleotide variant
(missense variant)
Alstrom syndrome
+2 more
GUncertain significance
ALMS1
(P2237L +1 more)
Single nucleotide variant
(missense variant)
Alstrom syndrome
+1 more
GUncertain significance
ALMS1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GConflicting classifications of pathogenicity
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