Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
TC/-|MAF: 0.08 (TC)
Location

Chromosome 11:108119642-108119643 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2510 sample genotypes.

Variant displays