Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.72195749T>CCA285750FOLR1c.493+2T>C (n.493+2T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.72195749T=CA1981880093FOLR1c.493+2T= (n.493+2T=)
dbSNP

Number of alleles fetched