Most severe consequence
21
Intron variant
Alleles
C/T|Ancestral: C
Location
Chromosome 11:2160544 (forward strand)|View in location tab
Evidence status 
Clinical significance
HGVS names
This variant has 8 HGVS names - Show
Synonyms
ClinVar RCV000258877
Original source
Variants of clinical significance imported from ClinVar (release 04/2017)|About ClinVar
About this variant
This variant overlaps 14 transcripts, 1 regulatory feature and is associated with 2 phenotypes.
