Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.27 (G)
Location

Chromosome 6:13275682 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs57949088

This variant has 10 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 12 transcripts and has 2513 sample genotypes.

Variant displays