Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 16:47696411 (forward strand) | View in location tab

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 28660_2

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 5 transcripts and is associated with 2 phenotypes.

Variant displays