Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.20 (G)
Location

Chromosome 11:68340003 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs170256, rs664003

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

About this variant

Variant displays