Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)
Location

Chromosome 1:11012522 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs17408916

This variant has 4 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 18 transcripts, 1 regulatory feature, has 3146 sample genotypes and is mentioned in 2 citations.

Variant displays