Original source

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

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

Chromosome 11:2128765 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58739087

HGVS name

11:g.2128765C>T

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 9 transcripts and has 3436 sample genotypes.

Variant displays