Original source

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

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: 0.46 (T)
Location

Chromosome 11:108346322 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, has 2695 sample genotypes and is mentioned in 1 citation.

Variant displays