Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (T)
Location

Chromosome 1:145926584 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs4483357

This variant has 9 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

Variant displays