Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
GTCAGTATCAATTCTGGAAGAATTTCCAGACA/-
Location

Chromosome 3:46373456-46373487 (forward strand) | View in location tab

Co-located

with COSMIC COSM1683921 (GTCAGTATCAATTCTGGAAGAATTTCCAGACA/-)

Most severe consequence
Evidence status

Clinical significance

Synonyms

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays