Original source

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

Alleles
G/T | Ambiguity code: K
Location

Chromosome 20:5304900 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs4392332

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

About this variant

This variant overlaps 1 transcript and has 2 sample genotypes.

Variant displays