Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59222428

HGVS name

9:g.2013580T>C

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 3697 individual genotypes and is associated with 1 phenotype.

Variation displays