Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.37 (G)
Location

Chromosome 2:233271764 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 13 HGVS names - click the plus to show

2:g.233271764A>G
ENST00000373525.9:c.276-1202A>G
ENST00000392017.8:c.708-1202A>G
ENST00000444735.5:c.276-1202A>G
ENST00000474148.5:n.835-1202A>G
ENST00000392021.7:c.*589-1202A>G
ENST00000498620.5:n.272-1202A>G
ENST00000479942.5:n.854-1202A>G
ENST00000347464.9:c.276-1202A>G
ENST00000419681.5:c.276-1202A>G
ENST00000392020.8:c.708-1202A>G
ENST00000417017.5:c.456-1202A>G
ENST00000392018.1:c.708-1202A>G

This variant has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 15 transcripts, has 3964 sample genotypes, is associated with 2 phenotypes and is mentioned in 16 citations.

Variant displays