Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.37 (C)
Location

Chromosome 9:2013580 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59222428

HGVS name

9:g.2013580T>C

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 9 transcripts, has 3697 sample genotypes and is associated with 1 phenotype.

Variant displays