Original source

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

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

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


with HGMD-PUBLIC CM951177

Most severe consequence
Stop gained
Evidence status

Clinical significance


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