Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

COSMIC COSM3689349

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

ClinVar SCV000171637

HGVS names

This variant has 3 HGVS names - Show

About this variant

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

Variant displays