Original source

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

Alleles
T/C/G|Ancestral: C|Ambiguity code: B|MAF: 0.19 (T)
Location

Chromosome 11:34470394 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3553 sample genotypes and is mentioned in 1 citation.

Variant displays