Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.03 (A)
Location

Chromosome 11:3806471 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 34 transcripts and has 2505 sample genotypes.

Variant displays