Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 11:34946472 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 270 sample genotypes.

Variant displays