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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130003565, RAB18
(V5L)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
RAB18
(Q67E +1 more)
Single nucleotide variant
(missense variant +2 more)
Warburg micro syndrome 3
GUncertain significance
RAB18
(P35S)
Single nucleotide variant
(missense variant +1 more)
Warburg micro syndrome 3
GUncertain significance
LOC130003565, RAB18
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
RAB18
Deletion
Warburg micro syndrome 3
GPathogenic
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