Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.02 (C)
Location

Chromosome 15:63059674 (forward strand) | View in location tab

Co-located

with COSMIC COSM3754394 (T/C), COSM3754392 (T/C), COSM3754395 (T/C), COSM3754393 (T/C), COSM3754391 (T/C)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 26 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 32 transcripts, has 2504 sample genotypes, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays