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Links from Gene

Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GREM1
Duplication
Familial colorectal cancer
GUncertain significance
GREM1
Duplication
Familial colorectal cancer
GUncertain significance
GREM1, SCG5
Duplication
Familial colorectal cancer
GUncertain significance
GREM1, GREM1-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GLikely benign
GREM1, GREM1-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GLikely benign
GREM1, GREM1-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GLikely benign
GREM1, SCG5
Duplication
Familial colorectal cancer
GUncertain significance
GREM1, SCG5
Duplication
Familial colorectal cancer
GUncertain significance
GREM1, SCG5
Duplication
Familial colorectal cancer
GUncertain significance
GREM1, GREM1-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign
GREM1, GREM1-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign
GREM1-AS1, GREM1
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
GREM1, SCG5
Duplication
Familial colorectal cancer
GUncertain significance
GREM1, SCG5
Duplication
Familial colorectal cancer
GUncertain significance
GREM1, SCG5
Duplication
Familial colorectal cancer
GUncertain significance
GREM1, SCG5
Duplication
Familial colorectal cancer
GUncertain significance
GREM1, SCG5
Duplication
Familial colorectal cancer
GPathogenic
GREM1, SCG5
Duplication
Familial colorectal cancer
GPathogenic
ARHGAP11A-SCG5, GREM1
+2 more
Duplication
Familial colorectal cancer
GUncertain significance
ARHGAP11A-SCG5, GREM1
+2 more
Duplication
Familial colorectal cancer
GPathogenic
ARHGAP11A-SCG5, GREM1
+3 more
Duplication
Familial colorectal cancer
GUncertain significance
ARHGAP11A-SCG5, GREM1
+2 more
Duplication
Familial colorectal cancer
GUncertain significance
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