Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.05 (G)
Location

Chromosome 1:2228951 (forward strand) | View in location tab

Co-located

with COSMIC COSM4143328 (C/G)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 2504 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays