Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)
Location

Chromosome 20:23637790 (forward strand) | View in location tab

Co-located

with COSMIC COSM3749695 (C/T)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 7 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 2505 sample genotypes, is associated with 2 phenotypes and is mentioned in 7 citations.

Variant displays