Original source

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

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.33 (C)
Location

Chromosome 20:41005726 (forward strand)|View in location tab

Most severe consequence
 
Regulatory region variant
Evidence status

Synonyms
HGVS name

20:g.41005726C>G

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 1 regulatory feature, has 3762 sample genotypes and is associated with 1 phenotype.

Variant displays