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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
3
g.138946431A>G
CA10654897
FOXL2
c.292T>C (p.Trp98Arg)
ClinVar
dbSNP
3
g.138946431A>T
CA354706977
FOXL2
c.292T>A (p.Trp98Arg)
dbSNP
Number of alleles fetched
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