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
A/C/G/T|Ancestral: A|Ambiguity code: N|MAF: 0.41 (G)
Location

Chromosome 1:150965185 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs17661590, rs386536884

HGVS names

This variant has 21 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, HumanOmniExpress

About this variant

This variant overlaps 69 transcripts and has 2751 sample genotypes.

Variant displays