Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.50 (A)
Location

Chromosome 11:47335319 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58205716

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 5 transcripts and has 2590 sample genotypes.

Variant displays