Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.08 (T)
Location

Chromosome 10:69401072 (forward strand) | View in location tab

Co-located

with COSMIC COSM4144807 (C/T), COSM4144809 (C/T), COSM4144808 (C/T), COSM4144810 (C/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3750791

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts and has 2836 individual genotypes.

Variation displays