Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.16 (C)
Location

Chromosome 11:116835627 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17249456

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2530 sample genotypes.

Variant displays