Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.48 (T)
Location

Chromosome 1:17045190 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs60946044

This variant has 8 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

Variant displays