Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.46 (T)
Location

Chromosome 4:186211877 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs17591572, rs3175017

This variant has 4 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 5 transcripts and has 3214 sample genotypes.

Variant displays