This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

Chromosome 17:43115792 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


LSDB U14680.1:c.81-13C>G, U14680.1:c.81-13C>A

HGVS names

This variant has 72 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 66 transcripts, has 2504 sample genotypes and is associated with 3 phenotypes.

Variant displays