Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.37 (T)
Location

Chromosome 11:3802168 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59974007

HGVS names

This variant has 20 HGVS names - Show

About this variant

Variant displays