Original source

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

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

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