This variant has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP
Note: The reference base for this variant (C) does not match the Ensembl reference base (G) at this location.
Chromosome 17:5441126 (forward strand) | View in location tab
Archive dbSNP rs386513029
This variant has 5 HGVS names - Show
This variant has assays on: Illumina_Human1M-duo