Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.43 (A)
Location

Chromosome 5:126543263 (forward strand) | View in location tab

Co-located

with dbSNP rs200532010 (A/C)

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant overlaps 5 transcripts and has 2511 sample genotypes.

Variant displays