Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 1:2228865 (forward strand) | View in location tab

Co-located

with COSMIC COSM3689349 (C/G)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

This variant has 2 HGVS names - click the plus to show

About this variant

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

Variant displays