Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.20 (T)
Location

Chromosome 1:153261102 (forward strand) | View in location tab

Co-located

with COSMIC COSM3748998 (C/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs4604649

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

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 2 transcripts and has 3498 individual genotypes.

Variation displays