Original source

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

G/A/C | Ancestral: C | Ambiguity code: V | MAF: 0.04 (G)

Chromosome 14:100829493 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs61660316

HGVS names

This variant has 30 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 52 transcripts and has 2782 sample genotypes.

Variant displays