Original source

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