Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: < 0.01 (G)
Location

Chromosome 11:108353970 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs569239

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2512 sample genotypes.

Variant displays