Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.31 (C)

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


with HGMD-PUBLIC CS077842

Most severe consequence
Evidence status

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

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 13 transcripts, has 2400 individual genotypes and is mentioned in 6 citations.

Variation displays