Original source

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

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

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

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

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