Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.41 (G)

Chromosome 4:155211064 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58071726, rs17376833

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 5 transcripts, has 3766 sample genotypes and is mentioned in 2 citations.

Variant displays