Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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