Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 3:41240239 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant

This variant has 5 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 9 transcripts and has 36 sample genotypes.

Variant displays