Original source

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

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

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

Co-located variant

HGMD-PUBLIC CM951177

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 15102

HGVS names

This variant has 24 HGVS names - 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