Original source

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

G/T | Ancestral: G | Ambiguity code: K

Chromosome 13:20048804 (forward strand) | View in location tab


with dbSNP rs528942001 (G/-)

Most severe consequence
Intron variant
HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts.

Variant displays