Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.37 (A)
Location

Chromosome 5:150860025 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56514338, rs60413553

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

5:g.150860025G>A
ENST00000520549.1:c.158+11371G>A

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

About this variant

This variant overlaps 1 transcript, has 2648 sample genotypes, is associated with 1 phenotype and is mentioned in 69 citations.

Variant displays