Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.48 (C)
Location

Chromosome 4:88962828 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59688598

This variant has 6 HGVS names - click the plus to show

4:g.88962828C>T
ENST00000511976.5:c.-22-24587G>A
ENST00000512339.5:c.428-24587G>A
ENST00000509094.5:c.606-24587G>A
ENST00000264344.9:c.606-24587G>A
ENST00000502459.5:n.1064-24587G>A

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, 2 regulatory features, has 3687 sample genotypes, is associated with 1 phenotype and is mentioned in 18 citations.

Variant displays