Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 11:62690396 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Stop gained
Evidence status

HGVS names

This variant has 20 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 24 transcripts and 1 regulatory feature.

Variant displays