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

Chromosome 12:52790216 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs386456831

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

Variant displays