Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.20 (T)
Location

Chromosome 3:170996681 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs61791068

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2508 sample genotypes.

Variant displays