Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

dbSNP rs200532010 (A/C)

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 3 HGVS names - 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