Original source

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

Alleles
G/-|Ancestral: G|MAF: 0.01 (-)
Location

Chromosome 11:128685061 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2505 sample genotypes.

Variant displays