Original source

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

Alleles
C/G | Ambiguity code: S | MAF: 0.32 (G)
Location

Chromosome 11:2305690 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57149132

This variant has 16 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

Variant displays