Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.04 (G)
Location

Chromosome 3:159947262 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59217415

HGVS names

This variant has 2 HGVS names - Hide

3:g.159947262A>G
ENST00000497452.5:n.1351-32788T>C

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2754 sample genotypes, is associated with 4 phenotypes and is mentioned in 20 citations.

Variant displays