Original source

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

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.28 (C)
Location

Chromosome 6:10420248 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58120572

HGVS name

6:g.10420248G>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2772 sample genotypes and is mentioned in 1 citation.

Variant displays