Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 11:18407649 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 23 transcripts and 1 regulatory feature.

Variant displays