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 (TC) at this location.
Chromosome 5:112817967-112817968 (forward strand) | View in location tab
This variation has 18 HGVS names - click the plus to show
This variant overlaps 20 transcripts.