This variant has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP
Note: The reference sequence for this variant (C) does not match the Ensembl reference sequence (CG) at this location.
Chromosome 1:155295855-155295856 (forward strand)|View in location tab
This variant has 7 HGVS names - Show
This variant overlaps 6 transcripts.