Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.19 (C)
Location

Chromosome 19:45865719 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57248860

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays