Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59217415

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

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

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2524 sample genotypes, is associated with 4 phenotypes and is mentioned in 20 citations.

Variant displays