Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.06 (C)
Location

Chromosome 11:102875061 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17296532, rs386563292

HGVS name

11:g.102875061T>C

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2562 sample genotypes and is mentioned in 25 citations.

Variant displays