Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.45 (C)
Location

Chromosome 5:126192299 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57121158, rs17584016

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

5:g.126192299C>T
ENST00000507428.1:n.266-778C>T
ENST00000450613.2:n.71+87432G>A

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 4571 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays