Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 19:11375788 (forward strand) | View in location tab

Co-located

with COSMIC COSM3362649 (C/G)

Most severe consequence
Evidence status

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

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts and has 3003 individual genotypes.

Variation displays