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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CORIN
(S579C +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
CORIN, LOC101927179
(S4fs)
Duplication
(frameshift variant)
Preeclampsia/eclampsia 5
+1 more
GConflicting classifications of pathogenicity
CORIN
(S472G +2 more)
Single nucleotide variant
(missense variant)
Preeclampsia/eclampsia 5
GPathogenic
CORIN
(K317E +1 more)
Single nucleotide variant
(missense variant)
Preeclampsia/eclampsia 5
GPathogenic
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