Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 11:6393680 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM951177

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 15102

This variant has 24 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 54 transcripts and is associated with 2 phenotypes.

Variant displays