Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:119184751 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

11:g.119184751C>T

About this variant

This variant overlaps 22 transcripts.

Variant displays