Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M
Location

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

Co-located variant

dbSNP rs5871218 (A/-)

Most severe consequence
 
3 prime UTR variant
HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, HumanCoreExome-12, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts.

Variant displays