Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.08 (G)
Location

Chromosome 2:111231795 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17808494

HGVS names

This variant has 4 HGVS names - Hide

2:g.111231795T>G
ENST00000609220.1:n.39-34601A>C
ENST00000609902.5:n.328+1833A>C
ENST00000439362.5:n.636+1833A>C

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3596 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays