Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.18 (A)
Location

Chromosome 2:118849894 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs117016850, rs386619812

HGVS name

2:g.118849894C>A

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 3583 sample genotypes and is mentioned in 1 citation.

Variant displays