Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.44 (-)
Location

Chromosome 11:102799765 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

This variant has 4 HGVS names - click the plus to show

11:g.102799765delC
ENST00000525739.6:n.682+1644delC
ENST00000371455.7:n.423+1644delC
ENST00000544704.1:n.443+1644delC

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2557 sample genotypes, is associated with 4 phenotypes and is mentioned in 65 citations.

Variant displays