Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.50 (T)
Location

Chromosome 11:120792654 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17245727, rs60428773

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3764 sample genotypes and is mentioned in 20 citations.

Variant displays