Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)
Location

Chromosome 11:34437314 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

11:g.34437314T>C

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2582 sample genotypes and is mentioned in 1 citation.

Variant displays