Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 2:27131672 (forward strand) | View in location tab

Co-located

with COSMIC COSM1019527 (G/A)

Most severe consequence
 
Splice donor variant
Evidence status

This variant has 10 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 17 transcripts and has 2504 sample genotypes.

Variant displays