Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 11:62690389 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance

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, 1 regulatory feature and is associated with 1 phenotype.

Variant displays