Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: 0.45 (G)
Location

Chromosome 8:127414148 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58153033

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 4 transcripts, has 2691 sample genotypes and is mentioned in 1 citation.

Variant displays