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
C/A/G/T|Ancestral: C|Ambiguity code: N|MAF: 0.01 (T)
Location

Chromosome 11:17509497 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB 28936191

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 2504 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays