Original source

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

Alleles
T/A|Ancestral: A|Ambiguity code: W|MAF: 0.27 (A)
Location

Chromosome 3:38740702 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61456652, rs52792395

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 1 transcript and has 3750 sample genotypes.

Variant displays