Original source

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

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

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


with HGMD-PUBLIC CS077842

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs386542121

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 11 transcripts, 2 regulatory features, has 3808 sample genotypes and is mentioned in 7 citations.

Variant displays