Original source

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

Alleles
C/T|Ambiguity code: Y|MAF: 0.22 (C)
Location

Chromosome 11:2307889 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3782056

HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2511 sample genotypes.

Variant displays