Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.40 (G)
Location

Chromosome 1:55038977 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59883310, rs56641626

HGVS names

This variant has 2 HGVS names - Hide

1:g.55038977G>A
LRG_275:g.4431G>A

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 2 transcripts, has 4614 sample genotypes, is associated with 5 phenotypes and is mentioned in 10 citations.

Variant displays