Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs3782056

This variation has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2511 individual genotypes.

Variation displays