Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.20 (T)
Location

Chromosome 11:5242453 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 3 HGVS names - Hide

11:g.5242453C>T
ENST00000454892.1:n.162-206G>A
ENST00000433329.1:n.312-206G>A

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, has 2848 sample genotypes and is mentioned in 7 citations.

Variant displays