Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.06 (C)
Location

Chromosome 1:116990269 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs1127221, rs3182867

This variant has 3 HGVS names - click the plus to show

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

About this variant

Variant displays