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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
12
g.68157629C>T
CA13649226
IFNG
c.366+284G>A (n.366+284G>A)
ClinVar
dbSNP
gnomAD v2
gnomAD v3
gnomAD v4
12
g.68157629C>A
CA2043752627
IFNG
c.366+284G>T (n.366+284G>T)
dbSNP
Number of alleles fetched
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