Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.47 (A)
Location

Chromosome 15:74036235 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3784559, rs3169098

This variant has 15 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 20 transcripts, has 3696 sample genotypes and is mentioned in 1 citation.

Variant displays