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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GREM1
(K26R)
Single nucleotide variant
(missense variant +1 more)
Hereditary mixed polyposis syndrome
GUncertain significance
GREM1
(R64W)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
GREM1
(I103V +2 more)
Single nucleotide variant
(missense variant)
Hereditary mixed polyposis syndrome
+1 more
GUncertain significance
GREM1
(N57H)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
ARHGAP11A-SCG5, SCG5
(R178* +2 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GUncertain significance
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