Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.46 (C)
Location

Chromosome 4:154591789 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR016061

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs28375882

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts and has 2557 sample genotypes.

Variant displays