Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.08 (T)

Chromosome 16:28902389 (forward strand) | View in location tab

Most severe consequence
Splice region variant
Evidence status


Archive dbSNP rs2234848

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts and has 2771 sample genotypes.

Variant displays