Original source

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

HGMD-PUBLIC CR016061

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs28375882

HGVS names

This variant has 2 HGVS names - 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