Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.05 (A)

Chromosome 1:204437853 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs56493419

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 5304 sample genotypes, is associated with 8 phenotypes and is mentioned in 2 citations.

Variant displays