Original source

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

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

Variant displays