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 11:116835994 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CD072343

Most severe consequence
 
Synonymous variant

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and 1 regulatory feature.

Variant displays