Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 4:53378299 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Synonyms

Archive dbSNP rs386452402

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 11 transcripts and has 2504 individual genotypes.

Variation displays