Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 11:108234836 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS077842

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays