Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.32 (A)
Location

Chromosome 19:10295959 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57414207

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_ImmunoChip

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2772 sample genotypes and is mentioned in 2 citations.

Variant displays