Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 4:146641920 (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_Human1M-duo

About this variant

This variant overlaps 2 transcripts and has 3103 sample genotypes.

Variant displays