Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.04 (G)
Location

Chromosome 14:100829493 (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 rs61660316

This variation has 15 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip, Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 26 transcripts and has 2782 individual genotypes.

Variation displays