Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)
Location

Chromosome 11:27655126 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant

This variant has 28 HGVS names - click the plus to show

About this variant

This variant overlaps 27 transcripts and has 2504 sample genotypes.

Variant displays