Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.20 (A)
Location

Chromosome 2:112829544 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS name

2:g.112829544A>G

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 3230 sample genotypes and is mentioned in 9 citations.

Variant displays