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Links from OMIM

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IL21, IL21-AS1
+1 more
(R40H)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
IL21
Single nucleotide variant
(synonymous variant)
IL21-related infantile inflammatory bowel disease
+2 more
GBenign
LOC126807147, IL21-AS1
+1 more
(L49P)
Single nucleotide variant
(missense variant)
IL21-related infantile inflammatory bowel disease
GPathogenic
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