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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GINS1, LOC130065587
Single nucleotide variant
(5 prime UTR variant +1 more)
Combined immunodeficiency due to GINS1 deficiency
GPathogenic
GINS1, LOC130065587
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
GINS1
(R83C)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
GINS1
(C152Y)
Single nucleotide variant
(missense variant +1 more)
Combined immunodeficiency due to GINS1 deficiency
GLikely pathogenic
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