Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.39 (T)
Location

Chromosome 11:71441212 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

This variant has 7 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 13 transcripts, has 2619 sample genotypes and is associated with 1 phenotype.

Variant displays