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

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

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

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

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

HGVS names

This variant has 75 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 69 transcripts, has 2504 sample genotypes and is associated with 5 phenotypes.

Variant displays