Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.07 (T)
Location

Chromosome 11:69809714 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57025302

HGVS name

11:g.69809714C>T

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2567 sample genotypes and is mentioned in 1 citation.

Variant displays