Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.11 (A)
Location

Chromosome 19:33498339 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3786919, rs61464660, rs253674

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3952 sample genotypes and is associated with 1 phenotype.

Variant displays