Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.21 (G)
Location

Chromosome 2:17933286 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17316374, rs61681394

HGVS names

This variant has 2 HGVS names - Hide

2:g.17933286A>G
ENST00000465292.5:n.305+15415A>G

About this variant

This variant overlaps 4 transcripts, has 2832 sample genotypes and is mentioned in 1 citation.

Variant displays