Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.46 (A)
Location

Chromosome 4:89796284 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2506 sample genotypes.

Variant displays