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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
21
g.45990257G>C
CA10606786
COL6A1
c.931-1G>C (n.931-1G>C)
ClinVar
dbSNP
21
g.45990257G>A
CA10604117
COL6A1
c.931-1G>A (n.931-1G>A)
ClinVar
dbSNP
Number of alleles fetched
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