Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.32 (C)
Location

Chromosome 11:108364109 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS077842

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386542121

This variant has 13 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 11 transcripts, 2 regulatory features, has 2568 sample genotypes and is mentioned in 7 citations.

Variant displays