Original source

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

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

Chromosome 8:132923397 (forward strand) | View in location tab

Co-located

with COSMIC COSM3785870 (C/T) ; HGMD-PUBLIC CM930703

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5576

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variation displays