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Links from MedGen

Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NRIP1
(A623V)
Single nucleotide variant
(missense variant)
Congenital anomalies of kidney and urinary tract 3
GUncertain significance
NRIP1
(E743K)
Single nucleotide variant
(missense variant)
Congenital anomalies of kidney and urinary tract 3
GUncertain significance
NRIP1
Single nucleotide variant
(synonymous variant)
Congenital anomalies of kidney and urinary tract 3
+1 more
GBenign
NRIP1
(P554S)
Single nucleotide variant
(missense variant)
Congenital anomalies of kidney and urinary tract 3
GUncertain significance
NRIP1
(T1152M)
Single nucleotide variant
(missense variant)
Congenital anomalies of kidney and urinary tract 3
+1 more
GLikely benign
NRIP1
Deletion
(nonsense)
Congenital anomaly of kidney and urinary tract
+1 more
GPathogenic
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