Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 11:116837018 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs9692, rs3209633, rs11542978

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and 1 regulatory feature.

Variant displays