Original source

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

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

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


with 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