Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.14 (A)
Location

Chromosome 4:122408207 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61164551

HGVS names

This variant has 4 HGVS names - Hide

4:g.122408207G>A
ENST00000388724.6:c.848+176G>A
ENST00000296513.6:c.848+176G>A
ENST00000388725.2:c.794+176G>A

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 4 transcripts, has 4029 sample genotypes, is associated with 4 phenotypes and is mentioned in 23 citations.

Variant displays