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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCC6
(G1302R +1 more)
Single nucleotide variant
(missense variant +1 more)
Arterial calcification, generalized, of infancy, 2
+3 more
GPathogenic/Likely pathogenic
ABCC6
(W1259fs +1 more)
Duplication
(frameshift variant +1 more)
Arterial calcification, generalized, of infancy, 2
+3 more
GPathogenic
ABCC6
(G1086S +1 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive inherited pseudoxanthoma elasticum
GLikely pathogenic
ABCC6
(R1164Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
ABCC6
(G989R +1 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive inherited pseudoxanthoma elasticum
+3 more
GUncertain significance
ABCC6
(G755R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GLikely pathogenic
ABCC6
(E422K +1 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive inherited pseudoxanthoma elasticum
+3 more
GUncertain significance
ABCC6
(Q378* +1 more)
Single nucleotide variant
(nonsense +1 more)
not provided
+4 more
GPathogenic
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