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: G|Ambiguity code: N|MAF: 0.14 (T)
Location

Chromosome 12:51199833 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs117225250, rs60862983

HGVS names

This variant has 15 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 30 transcripts and has 2868 sample genotypes.

Variant displays