Original source

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

Alleles
C/A|Ambiguity code: M
Location

Chromosome 11:114124557 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays