Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.44 (T)
Location

Chromosome 11:6390705 (forward strand) | View in location tab

Co-located

with COSMIC COSM1561696 (T/C), COSM1561695 (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_ExomeChip

About this variant

This variant overlaps 28 transcripts, has 2538 individual genotypes and is mentioned in 2 citations.

Variation displays