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 (TC) at this location.
Chromosome 8:48922547-48922548 (forward strand)|View in location tab
Archive dbSNP rs2735452
This variant has 2 HGVS names - Show