Original source

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

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.14 (C)

Chromosome 19:45864687 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs57491674

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

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 11 transcripts and has 1400 individual genotypes.

Variation displays