Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y
Location

Chromosome 2:232538565 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

2:g.232538565T>C

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays