Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

dbSNP rs200073353 (T/-)

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs1745501, rs58761937

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

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

About this variant

Variant displays