This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
G/A/C/T|Ancestral: G|Ambiguity code: N|MAF: 0.07 (A)
Location

Chromosome 11:17509599 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB 11913336

HGVS names

This variant has 24 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 21 transcripts, has 2575 sample genotypes and is associated with 1 phenotype.

Variant displays