Original source

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

HGVS names

This variant has 3 HGVS names - Hide

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

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3961 sample genotypes and is mentioned in 2 citations.

Variant displays