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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLIS2
Single nucleotide variant
(5 prime UTR variant)
not provided
GUncertain significance
GLIS2
Single nucleotide variant
(synonymous variant)
GLIS2-related condition
+1 more
GConflicting classifications of pathogenicity
GLIS2
Single nucleotide variant
(synonymous variant)
Nephronophthisis
+3 more
GBenign/Likely benign
GLIS2
(D80V)
Single nucleotide variant
(missense variant)
GLIS2-related condition
+4 more
GConflicting classifications of pathogenicity
GLIS2
Single nucleotide variant
(intron variant)
Nephronophthisis
+1 more
GConflicting classifications of pathogenicity
GLIS2
Single nucleotide variant
(synonymous variant)
Nephronophthisis
+4 more
GConflicting classifications of pathogenicity
GLIS2
Single nucleotide variant
(synonymous variant)
Nephronophthisis
+3 more
GBenign
GLIS2
Single nucleotide variant
(synonymous variant)
Nephronophthisis
+2 more
GBenign
GLIS2
Single nucleotide variant
(synonymous variant)
Nephronophthisis
+1 more
GConflicting classifications of pathogenicity
GLIS2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
GLIS2
Single nucleotide variant
(synonymous variant)
Nephronophthisis
+3 more
GBenign
GLIS2
(T492A)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign
GLIS2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GUncertain significance
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