Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.01 (C)
Location

Chromosome 4:174489876 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs386542154

HGVS name

4:g.174489876A>C

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 12 transcripts and has 3038 sample genotypes.

Variant displays