Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.40 (G)
Location

Chromosome 13:27620912 (forward strand) | View in location tab

Co-located

with dbSNP rs200073353 (T/-)

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs1745501, rs58761937

This variant has 4 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

Variant displays