Original source

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

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

Chromosome 11:2162628 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

11:g.2162628C>T

About this variant

This variant overlaps 20 transcripts and 1 regulatory feature.

Variant displays