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Links from Gene

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRIG2
Copy number loss
not provided
GUncertain significance
LRIG2
(M1I)
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
GUncertain significance
LRIG2
(Q553* +1 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
LRIG2
(I723fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
LRIG2
(P696H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LRIG2
(R941fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
LRIG2
(F228fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
LRIG2
(S523R +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
LRIG2
(E413* +1 more)
Single nucleotide variant
(nonsense)
not provided
GLikely pathogenic
CAPZA1, LINC01356
+12 more
Duplication
Primary amenorrhea
GUncertain significance
LRIG2
(R86W)
Single nucleotide variant
(5 prime UTR variant +1 more)
Urofacial syndrome 2
GUncertain significance
LRIG2
(H566Y +1 more)
Single nucleotide variant
(missense variant)
Urofacial syndrome 2
GUncertain significance
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