This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: < 0.01 (A)
Location

Chromosome 6:161973317 (forward strand) | View in location tab

Co-located

with COSMIC COSM98176 (G/A), COSM3722940 (G/A) ; HGMD-PUBLIC CM030926, CM983422

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11237, 11255

This variation has 45 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 21 transcripts, has 2504 individual genotypes and is associated with 4 phenotypes.

Variation displays