Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.48 (G)
Location

Chromosome 3:115639308 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59103249

This variant has 3 HGVS names - click the plus to show

3:g.115639308G>A
ENST00000393780.3:c.-259+15589G>A
ENST00000305124.10:c.30+15589G>A

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2686 sample genotypes and is mentioned in 2 citations.

Variant displays