Original source

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

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and 1 regulatory feature.

Variant displays