Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.10 (C)
Location

Chromosome 1:39896789 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

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

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts, has 2507 sample genotypes and is mentioned in 1 citation.

Variant displays