This variant 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 (C)
Location

Chromosome 17:4901944 (forward strand) | View in location tab

Co-located

with COSMIC COSM178997 (G/A) ; HGMD-PUBLIC CM962727

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

This variant has 15 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 39 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays