Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.37 (T)
Location

Chromosome 6:1614132 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58252855

HGVS name

6:g.1614132T>G

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

Variant displays