Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.08 (T)
Location

Chromosome 11:203788 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs117234720, rs58518031

HGVS names

This variant has 5 HGVS names - Hide

11:g.203788C>T
ENST00000382762.7:c.*1514G>A
ENST00000410108.5:c.168+1823G>A
ENST00000526963.1:n.166C>T
ENST00000325147.13:c.*1682G>A

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 14 transcripts, has 3817 sample genotypes, is associated with 2 phenotypes and is mentioned in 7 citations.

Variant displays