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

Co-located variant

HGMD-PUBLIC CD072343

Most severe consequence
 
Synonymous variant
HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and 1 regulatory feature.

Variant displays