Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.18 (T)
Location

Chromosome 3:137071697 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

HGVS name

3:g.137071697C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant has 2507 sample genotypes and is mentioned in 2 citations.

Variant displays