Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.27 (C)
Location

Chromosome 8:96161256 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Uniprot VAR_023599

HGVS name

8:g.96161256T>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

Variant displays