This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Note: The reference sequence for this variant (C) does not match the Ensembl reference sequence (GT) at this location.
Chromosome 13:48232492-48232493 (forward strand) | View in location tab
This variant overlaps 5 transcripts.