Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17316374, rs61681394

This variant has 2 HGVS names - click the plus to show

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