Original source

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

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

Chromosome 16:50742722 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 14 transcripts and 1 regulatory feature.

Variant displays