Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.29 (G)

Chromosome 12:20893941 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57123378

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts and has 3116 sample genotypes.

Variant displays